Method of using 4-amino 6-substituted mycophenolic acid and derivatives

ABSTRACT

The disclosed derivatives of mycophenolic acid are therapeutic agents advantageous in the treatment of disease states indicated for mycophenolic acid and/or mycophenolate mofetil and other immunosuppressant agents.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is related to the following co-pending applications: Ser. Nos. 08/198,749, Attorney Docket No. 27960, entitled "5-Substituted Derivatives of Mycophenolic Acid"; 08/198,817, Attorney Docket No. 27970, entitled "4-Amino Derivatives of Mycophenolic Acid" now U.S. Pat. No. 5,380,879; 08/198,732, Attorney Docket No. 27980, entitled "4-Amino Derivatives of 5-Substituted Mycophenolic Acid"; and 08/198,725, Attorney Docket No. 27990, entitled "6-Substituted Mycophenolic Acid and Derivatives" now U.S. Pat. No. 5,444,072 filed contemporaneously herewith and incorporated herein by reference.

FIELD OF THE INVENTION

The present invention relates to derivatives of mycophenolic acid in which the 4-hydroxy group has been replaced by 4-amino derivatives, and the 6-methoxy group has been replaced by other substituents. The invention includes natural and derivative side chains at the 5-position. The invention is also directed to formulations and methods for treatment.

BACKGROUND INFORMATION AND RELATED DISCLOSURES

Mycophenolic acid ("MPA") was initially described as a weakly-active antibiotic found in the fermentation broth of Penicillium brevicompactum, having the following structure. ##STR1##

MPA and certain related compounds, such as mycophenolate mofetil (the morpholinoethyl ester of MPA), having the following structure: ##STR2## have more recently been described as having particularly advantageous properties as immunosuppressant drugs.

Various derivatives of mycophenolic acid, their synthesis and uses in the treatment of autoimmune disorders, psoriasis, inflammatory diseases, including, in particular, rheumatoid arthritis, tumors, viruses, and for treatment of allograft rejection, are described in U.S. Pat. Nos. 4,686,234; 4,725,622; 4,727,069; 4,748,173; 4,753,935; 4,786,637; 4,808,592; 4,861,776; 4,868,153; 4,948,793; 4,952,579; 4,959,387; 4,992,467; 5,247,083; and U.S. patent application Ser. No. 07/927,260, filed Aug. 7, 1992.

As immunosuppressive agents, the previously described esters and derivatives of mycophenolic acid are useful in treating auto-immune related disorders, glomerulonephritis and hepatitis, and in preventing allograft rejection. As anti-inflammatory agents, they are useful in treating rheumatoid arthritis. As anti-tumor agents, they are useful in treating solid tumors and malignancies of lymphoreticular origins. See also U.S. Pat. Nos. 3,825,571 and 3,853,919; Japanese Pat. No. J 01290667; J. Med. Chem., 33(2), 833-8 (1990); Austr. J. Chem., 31(2), 353-64, (1978); and J. Antibiot., 29(3), 275-85, 286-91 (1976). The disclosed compounds are described as having anti-tumor, immunosuppressive, anti-viral, anti-arthritic and/or anti-psoriatic activities. The article by J. W. Patterson and G. Huang, Chemical Communications, 1579 (1991) describes synthetic methodology of interest with respect to such compounds.

The above-cited patents, publications, and the references/publications referenced therein, are all incorporated herein by reference.

SUMMARY OF THE INVENTION

Derivatives of mycophenolic acid and their esters and the pharmaceutically acceptable salts thereof, i.e. the compounds of Formula I: ##STR3## wherein: R¹ is hydrogen or lower alkyl;

R² is hydrogen, lower alkyl --C(O)R³, --C(O)NR⁴ R⁵, --C(O)₂ R⁶, or --SO₂ R³ ; in

which:

R³ is hydrogen, lower alkyl, halo lower alkyl or optionally substituted phenyl;

R⁴ is hydrogen, lower alkyl or optionally substituted phenyl;

R⁵ is hydrogen, lower alkyl or optionally substituted phenyl;

R⁶ is lower alkyl or optionally substituted phenyl; and

R⁷ is lower alkyl, cycloalkyl, fluorovinyl, difluorovinyl, trifluorovinyl, lower alkenyl, --C.tbd.C--R⁸, allyl, CHO, or CH₂ OR⁹ ;

in which:

R⁸ is hydrogen or lower alkyl, and

R⁹ is hydrogen or 4-methoxybenzyl; and

Z is a side chain selected from Formulae ZA, ZB, ZC, ZD, ZE, ZF, ZG, and ZH: ##STR4## wherein: Z¹ is hydrogen, lower alkyl, halo or CF₃ ;

Z² is hydrogen, lower alkyl, lower alkoxy, aryl, or --CH₂ Z¹³, where

Z¹³ is aryl or heteroaryl;

Z³ is hydrogen, lower alkyl, lower alkenyl, lower alkoxy, phenyl, or --S(O)_(m) Z¹², where

Z¹² is lower alkyl, and

m is 0, 1 or 2;

Z⁴ is hydrogen, lower alkyl, or phenyl,

or Z³ and Z⁴ taken together with the carbon to which they are attached form cycloalkyl of three to five carbon atoms; and

G is OH, lower alkoxy, lower thioalkyl, --NG¹ G², --O(CH₂)_(n) NG¹ G², or --O(CH₂)_(n) N═G³, where

n is an integer from 1 to 6,

G¹ is hydrogen or lower alkyl,

G² is hydrogen or lower alkyl, and

═G³ is lower alkylene of four to six carbon atoms, or lower alkylene of three to five carbon atoms plus one member that is --O--, --S--, or --N(G⁴)-- where G⁴ is hydrogen or lower alkyl; ##STR5## wherein: Z⁵ is hydrogen or lower alkyl;

Z⁸ is hydrogen or lower alkyl;

D¹ and D² together with their adjacent carbon atoms form an optionally substituted, saturated or unsaturated carbocyclic or heterocyclic ring of 3 to 7 atoms; and

G is as defined above; or ##STR6## wherein: Z⁵, Z⁸, and G are as defined above; or ##STR7## wherein: D³ is --CH₂ -- or --CH₂ CH₂ --; and

G is as defined above; or ##STR8## wherein: Z⁶ is hydrogen, lower alkyl, lower alkoxy, --COOH, --NH₂ or halo;

Z⁷ is hydrogen, lower alkyl, lower alkoxy or halo; and

Z⁵ and G are as defined above; or ##STR9## wherein: Z¹ and G are as defined above; or ##STR10## wherein: D³, Z², Z³, Z⁴ and G are as defined above; or ##STR11## wherein: D⁴ is --CH₂ --, --CH₂ CH₂ --, --CH₂ CH₂ CH₂ --, --O--, or --OCH₂ --; and

Z¹ and G are as defined above;

and the pharmaceutically acceptable salts thereof.

In another aspect, the invention relates to a pharmaceutical composition containing a therpeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt thereof admixed with at least one pharmaceutically acceptable excipient.

In still another aspect, the invention relates to a method of treating immune, inflammatory, tumor, proliferative, viral and psoriatic disorders in a mammal by administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt thereof.

DETAILED DESCRIPTION OF THE INVENTION

Definitions and General Parameters

The following definitions are set forth to illustrate and define the meaning and scope of the various terms used to describe the invention herein.

As used herein, the term "alkyl" refers to a fully saturated monovalent radical of one to twelve carbon atoms containing only carbon and hydrogen, and which may be a cyclic, branched or straight chain radical. This term is further exemplified by radicals such as methyl, ethyl, t-butyl, pentyl, cyclopentyl, cyclohexyl, heptyl, cycloheptyl and adamantyl.

The term "lower alkyl" refers to a monovalent alkyl radical of one to six carbon atoms. This term is further exemplified by such radicals as methyl, ethyl, n-propyl, isopropyl, cyclopropyl, n-butyl, t-butyl, i-butyl (or 2-methylpropyl), isoamyl, pentyl, cyclopentyl, i-pentyl, hexyl and cyclohexyl.

The term "lower alkenyl" refers to an unsaturated monovalent hydrocarbon radical of one to six carbon atoms. This term is further exemplified by such radicals as vinyl, prop-2-enyl, pent-3-enyl, and hex-5-enyl.

The term "halo" refers to fluoro and chloro, unless otherwise specified.

The term "halo lower alkyl" refers to a lower alkyl radical substituted with one or more chlorine or fluorine atoms. This term is further exemplified by such radicals as trichloromethyl, trifluoromethyl, dichloromethyl, fluoromethyl, difluoro-chloro-methyl, 3-chloropropyl and 4-trifluoro-2-chloro-butyl.

The term "halomethyl" refers to a methyl radical substituted with one or more chlorine and/or fluorine atoms. This term is further exemplified by such radicals as trichloromethyl, trifluoromethyl, dichloromethyl, fluoromethyl and difluorochloromethyl.

The term "lower alkylene" refers to a divalent alkyl radical of one to six carbon atoms. This term is further exemplified by such radicals as methylene, ethylene, n-propylene, i-propylene, n-butylene, t-butylene, i-butylene (or 2-methylpropylene), isoamylene, pentylene, and n-hexylene.

The term "alkoxy" means the group --OR wherein R is lower alkyl.

The term "lower alkanol" means an alcohol of the formula ROH where R is a lower alkyl. This term is further exemplified by such alcohols as methanol, ethanol, n-propanol, i-propanol, n-butanol, t-butanol, i-butanol (or 2-methylpropanol), pentanol, n-hexanol.

The moiety "--N═G³ " as defined represents a heterocycle radical such as pyrrolidino, piperidino, hexamethyleneimino, imidazolidino, thiazolidino, morpholino, thiomorpholino, piperazino, thiopentamethyleneimino, and the like.

The term "optionally substituted phenyl" refers to phenyl and mono-, di-, or tri-substituted phenyl, wherein the optional substituents are lower alkyl, lower alkoxy, hydroxy, trifluoromethyl, or halo. This term is further exemplified by such radicals as 2-chlorophenyl, 2-trifluoromethylphenyl, 4-methoxyphenyl, 4-chlorophenyl, 3,4-dimethoxyphenyl, 2-chloro-3,4-dimethoxyphenyl, 4-hydroxyphenyl, 4-methylphenyl, 3-t-butylphenyl, and 4-hexylphenyl.

The term "aryl" refers to a monovalent unsaturated aromatic carbocyclic radical having a single ring (e.g., phenyl) or two condensed rings (e.g., naphthyl), which can optionally be mono-, di- or tri-substituted, independently, with OH, COOH, lower alkyl, lower alkoxy, chloro, fluoro, trifluoromethyl and/or cyano.

The term "heteroaryl" refers to a monovalent aromatic carbocyclic radical having at least one heteroatom, such as N, O or S, within the ring, such as quinolyl, benzofuranyl, pyridyl, morpholinyl and indolyl, which can optionally be mono-, di- or tri-substituted, independently, with OH, COOH, lower alkyl, lower alkoxy, chloro, fluoro, trifluoromethyl and/or cyano. The term "optionally substituted, saturated or unsaturated carbocyclic or heterocyclic ring of 3 to 7 atoms" as used with reference to a side chain of Formula ZB encompases side chains of the following structures: ##STR12## where the line inside each respective ring indicates the optional presence of a double bond and X¹, X², X³, X⁴ and X⁵ can independently be --CHX^(a) --, --C(O)--, --C(N--X^(b))--, --C(N--NX^(d) X^(e))--, --O--, --S--, --S(O)--, --S(O)₂ -- or --NX^(c) --,

where

X^(a) is hydrogen, lower alkyl or forms a double bond;

X^(b) is acyl, carbamoyl or ureido;

X^(c) lower alkyl, C(O)X^(d), S(O)₂ X^(d) or C(O)NX^(d) X^(e) ; and

X^(d) and X^(e) are independently hydrogen or lower alkyl;

provided that if more than one heteroatom is present such heteroatoms are separated by at least one carbon atom. Thus, a sidechain of Formula ZB in which D¹ and D² together represent --CH₂ CH₂ CH₂ CH₂ --, and Z⁵ and Z⁸ are both hydrogen, would be named as a 2-[(2-ethylidene)-2-cyclohex-1-yl]acetic acid derivative. Likewise, a sidechain of Formula ZB in which D^(l) and D² together represent --CH₂ CH₂ OCH₂ --, and Z⁵ and Z⁸ are both hydrogen, would be named as a 2-[(2-ethylidene)-4-tetrahydropyran-3-yl]acetic acid derivative.

The term "optional" or "optionally" means that the subsequently described event or circumstance may or may not occur, and that the description includes instances in which said event or circumstance occurs and instances in which it does not. For example, "optionally substituted phenyl" means that the phenyl may or may not be substituted and that the description includes both unsubstituted phenyl and phenyl wherein there is substitution: "optionally" followed by "converting the free base to the acid addition salt" means that such conversion may or may not be carried out in order for the process described to fall within the invention, and the invention includes those processes wherein the free base is converted to the acid addition salt and those processes in which it is not.

A "pharmaceutically acceptable salt" may be any salt derived from an inorganic or organic acid or base. Salts may be derived from acids or bases.

The acid addition salts are derived from inorganic acids, such as hydrochloric acid, hydrobromic acid, sulfuric acid (giving the sulfate and bisulfate salts), nitric acid, phosphoric acid and the like, and organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, malic acid, malonic acid, succinic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, salicylic acid, p-toluenesulfonic acid, and the like.

The base addition salts are derived from inorganic bases such as sodium hydroxide, potassium hydroxide, lithium hydroxide, ammonia, calcium hydroxide, magnesium hydroxide and the like. Cations derived from organic bases include those formed from primary, secondary and tertiary amines, such as isopropylamine, diethylamine, trimethylamine, triethylamine, pyridine, cyclohexylamine, ethylene diamine, monoethanolamine, diethanolamine, triethanolamine, and the like.

As used herein, the term "inert organic solvent" or "inert solvent" means a solvent inert under the conditions of the reaction being described in conjunction therewith (including, for example, benzene, toluene, acetonitrile, tetrahydrofuran, diethyl ether, chloroform, methylene chloride, pyridine, xylene, dimethylformamide, 1,4-dioxane, dichloromethane, and the like).

As used herein, the term "treatment" or "treating" means any treatment of a disease in a mammal, and includes:

(i) preventing the disease, that is, causing the clinical symptoms of the disease not to develop;

(ii) inhibiting the disease, that is, arresting the development of clinical symptoms; and/or

(iii) relieving the disease, that is, causing the regression of clinical symptoms.

As used herein, the term "effective amount" means a dosage sufficient to provide treatment. This will vary depending on the patient and the treatment being effected.

"Isomers" are different compounds that have the same molecular formula.

"Stereoisomers" are isomers that differ only in the way the atoms are arranged in space.

"Enantiomers" are a pair of stereoisomers that are non-superimposable mirror images of each other. A 1:1 mixture of a pair of enantiomers is a "racemic" mixture. The term "(±)" is used to designate a racemic mixture where appropriate.

"Diastereoisomers" are stereoisomers that have at least two asymmetric atoms, but which are not mirror-images of each other.

The absolute stereochemistry is specified according to the Cahn-Ingold-Prelog R-S system. When the compound is a pure enantiomer the stereochemistry at each chiral carbon may be specified by either R or S. Resolved compounds whose absolute configuration is unknown are designated (+) or (-) depending on the direction (dextro- or laevorotary) which they rotate the plane of polarized light at the wavelength of the sodium D line.

When a compound is a racemic mixture the stereochemistry at each chiral carbon may be specified by either RS or SR by reference to a single enantiomer of the racemate. In this manner relative stereochemistry is conveyed unambiguously.

The compounds of the invention may possess one or more asymmetric centers, and can be produced as a racemic mixture or as individual enantiomers or diastereoisomers. The number of stereoisomers present in any given compound of Formula I depends upon the number of asymmetric centers present (there are 2^(n) stereoisomers possible where n is the number of asymmetric centers). The individual stereoisomers may be obtained by resolving a racemic or non-racemic mixture of an intermediate at some appropriate stage of the synthesis, or by resolution of the compound of Formula I by conventional means. The individual stereoisomers (including individual enantiomers and diastereoisomers) as well as racemic and non-racemic mixtures of stereoisomers are encompassed within the scope of the present invention, all of which are intended to be depicted by the structures of this specification unless otherwise specifically indicated. Specific examples of the separation of isomers are set forth in the Examples.

Unless specified to the contrary, the reactions described herein take place at atmospheric pressure over a temperature range from about -20° C. to about 100° C., more preferably from about 10° C. to about 50° C., and most preferably at about room temperature.

Isolation and purification of the compounds and intermediates described herein can be effected, if desired, by any suitable separation or purification procedure such as, for example, filtration, extraction, crystallization, column chromatography, thin-layer chromatography or thick-layer chromatography, or a combination of these procedures. Specific illustrations of suitable separation and isolation procedures can be found by reference to the examples hereinbelow. However, other equivalent separation or isolation procedures can, of course, also be used.

Nomenclature

The compounds of Formula I will be named using the numbering system illustrated below.

The isobenzofuranyl nucleus of the compounds of Formula I is numbered as follows: ##STR13## Following are examples of how some representative compounds of Formula I are named.

Sidechains of Formula ZA are numbered as shown below: ##STR14##

Representative compounds of Formula I where the sidechain is ZA are as follows:

    __________________________________________________________________________     # R.sup.1                                                                           R.sup.2                                                                              R.sup.7                                                                             Z.sup.1                                                                           Z.sup.2                                                                            Z.sup.3                                                                               Z.sup.4                                                                            G   Ismr                                     __________________________________________________________________________     1 H  H     CH.sub.3                                                                            CH.sub.3                                                                          H   H      CH.sub.3                                                                           OH  S                                        2 H  C(O)CF.sub.3                                                                         cyclo-                                                                              CH.sub.3                                                                          H   H      C.sub.2 H.sub.5                                                                    OH  S                                                   propyl                                                              3 H  CH.sub.3                                                                             vinyl                                                                               CF.sub.3                                                                          OH  NHSO.sub.2 CH.sub.3                                                                   C.sub.6 H.sub.5                                                                    OCH.sub.3                                                                          RS                                       4 H  C(O)NMe.sub.2                                                                        ethynyl                                                                             Cl CH.sub.3                                                                           SO.sub.2 CH.sub.3                                                                     H   SCH.sub.3                                                                          RS                                       __________________________________________________________________________

and are named:

1. (E)-6-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)-2(S), 4-dimethyl-4-hexenoic acid;

2. (E)-6-(6-cyclopropyl-1,3-dihydro-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-2(S)-ethyl-4-methyl-4-hexenoic acid;

3. methyl (E)-6-(1,3-dihydro-7-methyl-4-methylamino-3-oxo-6-vinylisobenzofuran-5-yl)-3-hydroxy-2-methylsulfonylamino-2-phenyl-4-trifluoromethyl-4-hexenoate;

4. thiomethyl (E)-4-chloro-6-(1,3-dihydro-4-(3,3-dimethylureido)-6-ethynyl-7-methyl-3-oxoisobenzofuran-5-yl)-3-methyl-2-methylsulfonyl-4-hexenoate.

Sidechains of Formula ZB in which D¹ and D² do not contain a hetero atom are numbered as shown below: ##STR15##

Representative compounds of Formula I where the sidechain is ZB in which D² does not include a hetero atom are as follows:

    __________________________________________________________________________     # R.sup.1                                                                           R.sup.2                                                                              R.sup.7  D.sup.1                                                                            D.sup.2                                                                              Z.sup.5                                                                            G    Ismr                                    __________________________________________________________________________     1 H  H     CH.sub.2 OH                                                                             CH.sub.2                                                                           CH.sub.2 CH.sub.2                                                                    H   OH   S                                       2 H  CH.sub.3                                                                             CH═CHF                                                                              (CH.sub.2).sub.2                                                                   CH.sub.2 CH.sub.2                                                                    H   OH   RS                                      3 H  C(O)CF.sub.3                                                                         CH.sub.2 CH═CH.sub.2                                                                (CH.sub.2).sub.2                                                                   (CH.sub.2).sub.3                                                                     CH.sub.3                                                                           NG.sup.1 G.sup.2                                                                    RS                                      4 H  C(O)NMe.sub.2                                                                        But-2-ynyl                                                                              CH.sub.2                                                                           CH.sub.2                                                                             Hexyl                                                                              SCH.sub.3                                                                           (1)-R                                   __________________________________________________________________________

and are named:

1. (E)-2-{2-[2-[1,3-dihydro-4-amino-6-hydroxymethyl-7-methyl-3-oxoisobenzofuran-5-yl]ethylidene]cyclopent-1-(S)-yl}acetic acid;

2. (E)-2-{2-[2-(1,3-dihydro-6-(2-fluorovinyl)-7-methyl-4-methylamino-3-isobenzofuran-5-yl)ethylidene]cyclohex-1-yl}acetic acid;

3. (E)-2-{2-[2-(1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)-4-trifluoroacetylaminoisobenzofuran-5-yl)ethylidene]cyclohept-1-yl}propionic acid dimethylamide (where G¹ and G² are both methyl);

4. thiomethyl (E)-2-{2-[2-(6-(but-2-ynyl)-1,3-dihydro-4-(3,3-dimethylureido)-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]-cyclobut-1-(R)-yl}octanoate.

Sidechains of Formula ZB that include a heteroatom are numbered differently, depending upon the position of the heteroatom(s) in the ring. For example, a sidechain of Formula ZB in which D¹ and D² together with their adjacent carbon atoms form a saturated heterocyclic ring of 6 atoms is numbered as shown below: ##STR16## where D represents --O--, --S(O)_(p) --, --N(R⁹)--, and the like.

Representative compounds of Formula I where the sidechain is ZB including a hetero atom are as follows:

    __________________________________________________________________________     # R.sup.1                                                                           R.sup.2                                                                             R.sup.7                                                                             D.sup.1 -D.sup.2                                                                         Z.sup.5                                                                             Z.sup.8                                                                           G     Ismr                                    __________________________________________________________________________     1 H  H    CH.sub.3                                                                            CH.sub.2 --O--CH.sub.2                                                                   H    H  OH    RS                                      2 H  C(O)CF.sub.3                                                                        CHO  (CH.sub.2).sub.2 --NH--CH.sub.2                                                          CH.sub.3                                                                            CH.sub.3                                                                          O-Hexyl                                                                              (3)-S                                   3 H  CH.sub.3                                                                            C.sub.2 H.sub.5                                                                     (CH.sub.2).sub.2 --S--CH.sub.2                                                           Hexyl                                                                               H  NG.sup.1 G.sup.2                                                                     RS                                      __________________________________________________________________________

and are named:

1. (E)-2-{4-[2-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)ethylidene]tetrahydrofuran-3-yl}acetic acid;

2. hexyl (E)-2-{4-[2-(1,3-dihydro-6-formyl-7-methyl-3-oxo-4-trifluoroacesobenzofuran-5-yl)ethylidene]-3-methylpiperidin-3(S)-yl}propionate;

3. (E)-2-{4-[2-(1,3-dihydro-6-ethyl-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)ethylidene]thiepan-3-yl}heptanoic acid dimethylamide (where G¹ and G² are both methyl).

Sidechains of Formula ZC are numbered as shown below: ##STR17##

Representative compounds of Formula I where the sidechain is ZC are as follows:

    __________________________________________________________________________     #  R.sup.1                                                                          R.sup.2                                                                              R.sup.7                                                                              Z.sup.5                                                                             Z.sup.8                                                                           G        Isomer                                       __________________________________________________________________________     1  H H     CH.sub.3                                                                             CH.sub.3                                                                            H  OH       S                                            2  H C(O)CF.sub.3                                                                         CH.sub.2 OMB                                                                         H    H  O-Hexyl  RS                                           3  H CH.sub.3                                                                             cyclo-                                                                               CH.sub.3                                                                            i-Pr                                                                              OH       2-S, 1-S                                                hexyl                                                               4  H H     n-C.sub.3 H.sub.7                                                                    Hexyl                                                                               H  O(CH.sub.2).sub.2 NG.sup.1 G.sup.2                                                      RS                                           __________________________________________________________________________

and are named:

1. 3-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-enyl-1-(S)-acetic acid;

2. hexyl 3-(1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-ylmethyl)cyclopent-2-enyl-1-acetate;

3. 2-(S)-[3-(6-cyclohexyl-1,3-dihydro-7-methyl-4-methylamino-3-oxoisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1(S)-yl]-3-methylbutyric acid;

4. 2-dimethylaminoethyl 3-(4-amino-1,3-dihydro-7-methyl-3-oxo-6-propylisobenzofuran-5-ylmethyl)-2-hexylcyclopent-2-en-1-ylacetate (where G¹ and G² are both methyl).

Sidechains of Formula ZD are numbered as shown below: ##STR18##

Representative compounds of Formula I where the sidechain is ZD are as follows:

    ______________________________________                                         #   R.sup.1                                                                               R.sup.2  R.sup.7 D.sup.3                                                                               G       Isomer                              ______________________________________                                         1   H      H        CH.sub.3                                                                               CH.sub.2                                                                              OH      R                                   2   H      C(O)CF.sub.3                                                                            C.sub.2 H.sub.5                                                                        CH.sub.2 CH.sub.2                                                                     O-Hexyl RS                                  3   H      Methyl   CF═CF.sub.2                                                                        CH.sub.2                                                                              S-Methyl                                                                               RS                                  ______________________________________                                    

and are named:

1. (E)-3-[2-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopentane-1-(R)-carboxylic acid;

2. hexyl (E)-4-[2-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)ethylidene]cyclohexane-1-carboxylate;

3. methyl (E)-3-[2-(1,3-dihydro-7-methyl-4-methylamino-3-oxo-6-trifluorovinylisobenzofuran-5-yl)ethylidene]cyclopentane-1-thiocarboxylate.

Sidechains of Formula ZE are numbered as shown below: ##STR19##

Representative compounds of Formula I where the sidechain is ZE are as follows:

    ______________________________________                                         #   R.sup.1                                                                              R.sup.2  R.sup.7                                                                              Z.sup.5                                                                              Z.sup.6                                                                              Z.sup.7                                                                               G                                  ______________________________________                                         1   H     H        CH.sub.3                                                                             CH.sub.3                                                                             H     H      OH                                 2   H     C(O)CF.sub.3                                                                            s-Butyl                                                                              H     6-CH.sub.3                                                                           H      NG.sup.1 G.sup.2                   3   H     CH.sub.3 Allyl Hexyl 6-Cl  4-OCH.sub.3                                                                           O-Hexyl                            ______________________________________                                    

and are named:

1. (E)-2-[3-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)-1-methylprop-1-en-1-yl]benzoic acid;

2. (E)-2-[3-(6-sec-butyl-1,3-dihydro-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)prop-1-en-1-yl]-6-methylbenzoic acid dimethylamide (where G¹ and G² are both methyl);

3. hexyl (E)-6-chloro-2-[3-(6-allyl-1,3-dihydro-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)-1-hexylprop-1-en-1-yl]-4-methoxybenzoate.

Sidechains of Formula ZF are numbered as shown below: ##STR20##

Representative compounds of Formula I where the sidechain is ZF are as follows:

    ______________________________________                                         #    R.sup.1                                                                              R.sup.2   R.sup.7                                                                               Z.sup.1                                                                               G      Isomer                               ______________________________________                                         1    H     H         CH.sub.3                                                                              Methyl OH     S                                    2    H     C(O)CF.sub.3                                                                             C.sub.2 H.sub.5                                                                       Hexyl  O-Ethyl                                                                               RS                                   3    H     Methyl    cyclo- H      S-Methyl                                                                              RS                                                        pentyl                                                    ______________________________________                                    

and are named:

1. 4-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-(S)-carboxylic acid;

2. ethyl 4-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-ylmethyl)-3-hexylcyclopent-3-ene-1-carboxylate;

3. thiomethyl 4-(6-cyclopentyl-1,3-dihydro-7-methyl-4-methylamino-3-oxoisobenzofuran-5-ylmethyl)cyclopent-3-ene-1-carboxylate.

Sidechains of Formula ZG are numbered as shown below: ##STR21##

Representative compounds of Formula I where the sidechain is ZG are as follows:

    ______________________________________                                         #    R.sup.1                                                                              R.sup.2                                                                               R.sup.7                                                                             D.sup.3                                                                             Z.sup.2                                                                             Z.sup.3                                                                             Z.sup.4                                                                              G    Isomer                        ______________________________________                                         1    H     H      CH.sub.3                                                                            CH.sub.2                                                                            H    H    H     OH   (3)-S                         2    H     CH.sub.3                                                                              C.sub.2 H.sub.5                                                                     CH.sub.2                                                                            CH.sub.3                                                                            CH.sub.3                                                                            Phenyl                                                                               OH   RS                            ______________________________________                                    

and are named:

1. 3-[3-(S)-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzo-furan-5-yl)cyclopent-1-en-1-yl]-propionic acid;

2. 3-[3-(1,3-dihydro-6-ethyl-7-methyl-4-methylamino-3-oxo-isobenzofuran-5-yl)cyclopent-1-en-1-yl]-2,3-dimethyl-2-phenyl propionic acid.

Sidechains of Formula ZH are numbered as shown below: ##STR22##

Representive compounds of Formula I where the sidechain is ZH are shown as follows:

    ______________________________________                                         #   R.sup.1                                                                              R.sup.2  R.sup.7 D.sup.4                                                                              Z.sup.1                                                                              G     Isomer                            ______________________________________                                         1   H     H        CH.sub.3                                                                               CH.sub.2                                                                             Methyl                                                                               OH    RS                                2   H     C(O)CF.sub.3                                                                            C.sub.2 H.sub.5                                                                        (CH.sub.2).sub.2                                                                     Methyl                                                                               O-    1-R                                                                      Ethyl                                   3   H     Methyl   CH.sub.2 OCH.sub.3                                                                     (CH.sub.2).sub.3                                                                     H     S-    RS                                                                       Methyl                                  ______________________________________                                    

are named as follows:

1. (E)-2-[3-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)-1-methylprop-1-en-1-yl]cyclopentane-1-carboxylic acid;

2. Ethyl (E)-2-[3-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-1-methylprop-1-en-1-yl]cyclohexane-1R-carboxylate;

3. Thiomethyl (E)-2-[3-(1,3-dihydro-6-methoxymethyl-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)prop-1-en-1-yl]cycloheptane-1-carboxylate.

Compounds of Formula I where the side chain is ZH, in which D⁴ is a heteroatom, are numbered differently, in that the heteroatom is designated as position 1 of the ring. For example, the compound where D⁴ is oxygen, and R¹ and R² are both hydrogen, R⁷ is methyl, Z¹ is methyl, and G is hydroxy, is named as follows:

(E)-2-[3-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)-1-methylprop-1-en-1-yl]furan-3-carboxylic acid.

PREPARATION OF COMPOUNDS OF FORMULA I

The compounds of Formula I are prepared from the lower alkyl 4-isocyanato esters of Formula 6, the structure of which is shown below: ##STR23## where Z^(a) is a sidechain of Formula Z as defined in the Summary of the Invention in which G is lower alkoxy.

The compounds of Formula 6 are prepared from intermediates of Formula A: ##STR24## where Z^(a) is as defined above. The preparation of compounds of Formula A is illustrated below in Reaction Scheme XXIII.

The compounds of Formula 6 are then converted to the compounds of Formula I by several different synthetic pathways, depending on the desired substitutions at the 4-position.

Many of the esterification routes and/or final esterification steps for the esters of the 4-substituted derivatives of mycophenolic acid are described in U.S. Pat. Nos. 4,686,234; 4,725,622; 4,727,069; 4,748,173; 4,753,935; 4,861,776; and the pending application entitled "Direct Esterification of Mycophenolic Acid", Ser. No. 07/911635, filed Jul. 10, 1992 (by inventors working in the same research organization as that of the present applicants, and subject to an obligation of assignment to the same assignee as in the present application) all previously incorporated herein by reference. By substituting the acids of Formula I for mycophenolic acid or its acid derivatives as described in the above references, the esterification routes and/or final steps described may likewise be used.

Starting Materials

The intermediates of Formula A are prepared starting from compounds of Formula 1, the structure of which is shown below: ##STR25## where Z^(a) is as defined above.

The compounds of Formula I may be prepared as described below in Reaction Schemes I to XXII. The preparation of such compounds is also described in more detail in co-pending application Ser. No. 08/198,749, Attorney Docket No. DO-MPA-1, filed contemporaneously herewith, which is hereby incorporated by reference in its entirety.

As those skilled in the art will appreciate, the intermediates synthesized in the preparation of compounds of Formula 1, e.g., where R^(a) is tosyl and/or where G is lower alkoxy can be substituted in Reaction Scheme XXIII for the compounds of Formula 1 and B without need for conversion through corresponding compounds where R^(a) is H and G is OH. For example, the compounds of Formula 105 where R^(a) is aryl or alkylsulfonyl can be used directly as compound of Formula 2 in Reaction Scheme XXIII.

Alternatively, when R⁷ is lower alkyl or cycloalkyl, by using mycophenolic acid as the starting material and performing the syntheses described with reference to Reaction Schemes XXIII and XXIV, the correspondingly obtained 6-substituted derivatives can be further derivatized at the 4- and/or 5-position(s), e.g., as described with reference to Reaction Schemes I through XXII.

Starting Materials

Mycophenolic acid is commercially available, e.g., from Sigma Chemical Company, St. Louis, Mo. The mycophenolic acid lower alkyl esters of Formula 1 can be synthesized, for example, as described in Synthetic Organic Chemistry by Wagner and Zook (Wiley, N.Y.) 1956, see pages 479-532. Other reactants, such as methoxyethoxy methyl chloride, t-butyl-dimethylsilyl chloride, and various orthoesters are likewise commercially available or may be readily prepared by those skilled in the art using commonly employed synthetic methodology.

Preparation of Compounds of Formula 1 where Z is Sidechain ZA

One method of preparing compounds of Formula 1 where Z is the sidechain of Formula ZA, illustrated as compounds of Formula 1A, is shown below in Reaction Schemes I to X. ##STR26## Preparation of Formula 102

As illustrated in Reaction Scheme I, Step 1, the phenolic hydroxyl group of a mycophenolic acid lower alkyl ester is protected.

A mycophenolic acid lower alkyl ester of Formula 101, in a solvent (such as ether, ethyl acetate, dimethyformamide, or preferably dichloromethane), is reacted with an equimolar amount of a halogenated protecting group (such as: methoxyethoxymethyl chloride; a sulfonyl chloride, e.g., tosyl chloride, mesyl chloride; or a silyl chloride, e.g., trimethylsilyl chloride, diphenylmethylsilyl chloride, or preferably tert-butyldimethylsilyl chloride) in presence of an equimolar amount of an organic base (such as diisopropylethylamine, triethylamine or imidazole). The reaction takes place at -20° to 35° C. (preferably at 25° C.) for 1 to 24 hours (preferably 16 hours) to give the corresponding compound of Formula 102 (where R^(a) is the protecting group).

Preparation of Formula 103

As illustrated in Reaction Scheme I, Step 2, the side chain double bond of a protected mycophenolic acid lower alkyl ester is ozonized to yield an aldehyde.

A stream of ozonized oxygen is passed through a solution of a protected compound of Formula 102 in a solvent (such as an alcohol, a halocarbon, or preferably a mixture of methanol and dichloromethane). The reaction takes place at -100° to -40° C. (preferably at -80° C.), and continues until the presence of excess ozone is detected by the development of a blue color. The resultant hydroperoxide reduced without further purification, by the addition of a reducing agent (such as zinc and acetic acid, dimethyl sulfide, or preferably thiourea). The reaction takes place at -80° C. to 25° C. (preferably 0° C.) over a period of 12 to 24 hours (preferably 16 hours), to give the corresponding aldehyde of Formula 103.

Preparation of Formula 104

As illustrated in Reaction Scheme I, Step 3, the aldehyde is converted to a carbinol by addition of an organometallic compound of Formula 103a [where M is MgBr or lithium, preferably MgBr (a Grignard reagent); Z¹ is hydrogen, lower alkyl or CF₃, and Z² is hydrogen or lower alkyl].

An organolithium reagent is formed by reaction of a halovinyl (preferably bromovinyl) compound of Formula 103a (where M is halo) with an alkyllithium (preferably n-butyllithium) in an ethereal solvent (such as ether, or preferably tetrahydrofuran). The reaction takes place at -100° to 0° C. (preferably -40° C.) over a period of 0.5 to 5 hours (preferably 1 hour).

Alternatively the halovinyl compound of Formula 103a is reacted with magnesium metal in an ethereal solvent (such as ether or preferably tetrahydrofuran). The reaction takes place at 30° to 60° C. (preferably 40° C.) over a period of 1 to 6 hours (preferably 2 hours).

The organometallic compound of Formula 103a where M is zinc or cadmium may be prepared by reaction of 103a where M is Li or MgBr with a zinc or cadmium halide, preferably chloride. The compound of Formula 103a where M is tin may be prepared by reaction of 103a where M is Li or MgBr with a trialkyl chlorostannane, preferably tributyltin chloride. The compound of Formula 103a where M is tin may also be prepared by reaction of 103a where M is trifluoromethanesulfonate by reaction with a compound of formula (R₃ Sn)₂, where R is alkyl, preferably metal, in the presence of a palladium catalyst, preferably tetrakis(triphenylphosphine)palladium. The compound of Formula 103a where M is trifluoromethanesulfonate may be prepared from a ketone of the formula: ##STR27## by reaction with a strong base (such as sodium hydride or potassium hexamethyldisilazide), followed by reaction of the anion thus produced with trifluoromethanesulfonic anhydride. Alternatively, the compound of Formula 103a where M is tin may be prepared by reacting a trialkyl tin hydride (preferably tributyl tin hydride) with an acetylene of the formula Z¹ --C.tbd.C--Z².

One molar equivalent of the resultant organometallic reagent is added to a solution of an aldehyde of Formula 103 (in the same solvent system used to make the organometallic reagent). The reaction takes place at -80° to 20° C. (preferably 0° C.) over a period of 5 to 60 minutes (preferably 10 minutes) to give the corresponding carbinol of Formula 104.

Preparation of Formula 105

As illustrated in Reaction Scheme I, Step 4, an alkyl ester of Formula 105 is formed by a Claisen ortho ester rearrangement reaction of a carbinol of Formula 104 and an orthoester of Formula 104a (where Z³ is hydrogen, halo, lower alkyl, lower alkenyl, phenyl, alkoxy or- thio lower alkyl; and Z⁴ is hydrogen or lower alkyl; or Z³ and Z⁴ taken together with the carbon to which they are attached form cycloalkyl).

A carbinol of Formula 104 is heated at 50° to 140° C. (preferably about 130° C.) with about 10 molar equivalents of an orthoester of Formula 104a, in the presence of from 0.05 to 0.25 molar equivalents (preferably 0.10 molar equivalents) of an organic acid catalyst (such as propionic, butyric, or preferably trimethylacetic acid). The reaction takes place over a period of 1 to 48 hours (preferably 3 hours) to give the corresponding alkyl ester of Formula 105.

Preparation of Formula 1A

Compounds of Formula 1A are prepared as esters by deprotection of compounds of Formula 105 as described below with reference to Reaction Scheme X, Step 1; they are hydrolyzed to the corresponding carboxylic acid as described below with reference to Reaction Scheme X, Step 2.

Preparation of Enantiomers of Formula 1A where Z² is Lower Alkyl

One method of preparing individual enantiomers of compounds of Formula 1A is from chiral compounds of Formula 104b, the preparation of which is shown below in Reaction Scheme II. ##STR28## where Y is chloro or bromo. ##STR29## Preparation of Formula 103f

As illustrated in Reaction Scheme II, Step 1, an aldehyde of Formula 103 is oxidized to the corresponding carboxylic acid of Formula 103f.

An aldehyde of Formula 103 is reacted with about two molar equivalents of an oxidizing agent (for example, chromic acid, silver oxide, bleach, or preferably sodium periodate), in an inert solvent (such as toluene, or preferably ethyl acetate), in the presence of water and a catalytic amount (for example, about 0.01 molar equivalents) of a catalyst (such as ruthenium oxide, or preferably ruthenium trichloride). The reaction takes place at 0° to 40° C. (preferably 25° C.) for 30 minutes to 8 hours (preferably 2 hours), to give the corresponding carboxylic acid of Formula 103f.

Preparation of Formula 103g

As illustrated in Reaction Scheme II, Step 2, a carboxylic acid of Formula 103f is converted to the corresponding acyl halide of Formula 103g.

A carboxylic acid of Formula 103f is reacted with about one molar equivalent, preferably 1.1 molar equivalents, of a halogenating agent (for example, thionyl chloride, thionyl bromide, or preferably oxalyl chloride), in an inert solvent (such as dichloromethane, or preferably ethyl acetate), in the presence of a catalytic amount (for example, about 0.05 molar equivalents) of dimethylformamide. The reaction takes place at 0° to 40° C. (preferably 25° C.) for 30 minutes to 8 hours (preferably 2 hours), to give the corresponding acyl halide of Formula 103g.

Preparation of Formula 103h

As illustrated in Reaction Scheme II, Step 3, an acyl halide of Formula 103g is converted to the corresponding keto olefin of Formula 103h by addition of an organometallic compound of Formula 103a.

An acyl halide of Formula 103g is reacted with about one molar equivalent of a organometallic compound of Formula 103a (where M is cadmium, zinc, tin, or the like, prepared as shown in the preparation of compounds of Formula 104), in an inert solvent (such as dichloromethane, ether, or preferably tetrahydrofuran), optionally in the presence of a catalytic amount (for example, about 0.05 molar equivalents) of a palladium catalyst [preferably tetrakis(triphenylphosphine)palladium]. The reaction takes place at -10° to 20° C. (preferably 0° C.) for 30 minutes to 8 hours (preferably 4 hours), to give the corresponding keto olefin of Formula 103h.

Preparation of Formula 104b

As illustrated in Reaction Scheme II, Step 4, a keto olefin of Formula 103h is reduced stereospecifically to the corresponding carbinol of Formula 104b by reduction with borane methyl sulfide in the presence of a catalytic amount of (R)-tetrahydro-1-methyl-3,3-diphenyl-1H,3H-pyrrolo-[1,2-c][1,3,2]oxazaborole.

A keto olefin of Formula 103h is sterospecifically reduced with about one molar equivalent of borane methyl sulfide in the presence of a catalytic amount (0.05-0.3 molar equivalents) of (R)-tetrahydro-1-methyl-3,3-diphenyl-1H,3H-pyrrolo-[1,2-c][1,3,2]oxazaborole in an inert solvent (preferably a mixture of toluene and dichloromethane). The reaction takes place at -30° to 40° C. (preferably -20° C.) for 1-24 hours (preferably 12 hours), to give the corresponding carbinol of Formula 104b.

Preparation of Enantiomers of Compounds of Formula 1A

The chiral carbinol of Formula 104b is then converted to an enantiomer of a compound of Formula 1A in the same manner as shown above in Reaction Scheme I (conversion of compounds of Formula 104 to 105 to 1A).

Preparation of Compounds of Formula 1A where Z² is Hydroxy

Compounds of Formula 1A where Z² is hydroxy are prepared as shown below in Reaction Scheme III. ##STR30## Preparation of Formula 106

As illustrated in Reaction Scheme III, Step 1, an aldehyde of Formula 103 is transformed into an unsaturated aldehyde of Formula 106 by a Wittig reaction with an ylid of Formula 103b (where Z¹ is hydrogen or lower alkyl).

An aldehyde of Formula 103 is reacted with one molar equivalent of an ylid of Formula 103b, in an organic solvent (such as dichloromethane, dimethylformamide or preferably toluene). The reaction takes place at 0° to 110° C. (preferably 80° C.) for 1 to 24 hours (preferably 8 hours) to give the corresponding unsaturated aldehyde of Formula 106.

Preparation of Formula 107

As illustrated in Reaction Scheme III, Step 2, an unsaturated aldehyde of Formula 106 is condensed with the anion of an ester of Formula 106a (where Z³ is hydrogen, lower alkyl, lower alkenyl, or phenyl and Z⁴ is hydrogen, lower alkyl, or phenyl) to give a beta-hydroxy ester of Formula 107.

An ester of Formula 106a is converted to an alkali metal salt by reacting a solution of the ester in an ethereal solvent (such as ether or preferably tetrahydrofuran) with an equimolar amount of an alkali metal hydride, hexamethyldisilazide or amide (preferably lithium diisopropylamide) at a temperature of -100° to 0° C. (preferably -80° C.), for 30 minutes to 2 hours (preferably 30 minutes) to give a solution of the corresponding ester anion. The ester anion solution (1.0 to 1.5 molar equivalents, preferably 1.0 molar equivalents) is added to a solution of an unsaturated aldehyde of Formula 106 in the same ethereal solvent. The condensation reaction takes place at a temperature of -100° C. to 0° C. (preferably -80° C.) for 1 to 6 hours (preferably 2 hours) to give the corresponding beta-hydroxy ester of Formula 107.

Preparation of Compounds of Formula 1A where Z² is Alkoxy

Compounds of Formula 1A where Z² is alkoxy are prepared as shown below in Reaction Scheme IV. ##STR31## Preparation of Formula 108

As illustrated in Reaction Scheme IV, Step 1, the beta-hydroxy group of an ester of Formula 107 is O-alkylated to give the corresponding beta-alkoxy ester (R^(b)) of Formula 108.

An ester of Formula 107 is reacted with 1 to 3 (preferably 1.5) molar equivalents of an alkyl halide (preferably an alkyl iodide, such as methyl iodide or n-butyl iodide, preferably methyl iodide) and 1 to 3 (preferably 1.25) molar equivalents of silver oxide, in a polar organic solvent (such as dioxane, dimethylformamide or preferably acetonitrile). The reaction takes place at 25° to 100° C. (preferably 70° C.) for 1 to 24 hours (preferably 4 hours) to give the corresponding beta-alkoxy ester of Formula 108.

Preparation of Compounds of Formula 1A where Z⁴ is Hydroxy

Compounds of Formula 1A where Z⁴ is hydroxy are prepared as shown below in Reaction Scheme V. ##STR32## Preparation of Formula 1A where Z⁴ is Hydroxy

As illustrated in Reaction Scheme V, Step 1, an alpha-halo alkyl ester of Formula 105 (where Z¹ is hydrogen, lower alkyl or CF₃, Z² is hydrogen or lower alkyl, Z³ is hydrogen, lower alkyl, lower alkenyl, or phenyl, and Z⁴ is halo) is converted to an alpha-hydroxy acid of Formula 1A where Z⁴ is hydroxy. The reaction takes place by hydrolysis of an alpha-alkanoyloxy ester intermediate, formed by displacement of the alpha-halo group with an alkali metal alkanoate.

An alpha-halo (preferably chloro) ester of Formula 105 is reacted with 1 to 5 (preferably 3) molar equivalents of an alkali metal alkanoate (the metal preferably potassium and the alkanoate preferably acetate) in a polar organic solvent (such as acetonitrile or preferably dimethylformamide) The reaction takes place at 40° to 100° C. (preferably 75° C.) for 1 to 24 hours (preferably 12 hours) to give the corresponding alpha-alkanoyloxy ester intermediate (not shown), which is employed without isolation or further purification.

The alpha-alkanoyloxy ester is then subjected to basic hydrolysis by reaction with 1 to 5 (preferably 2) molar equivalents of an alkali metal hydroxide (preferably sodium hydroxide) in a mixture of water and an organic solvent (such as methanol, dimethoxyethane or preferably tetrahydrofuran). The reaction takes place at 0° to 60° C. (preferably 40° C.) for 1 to 12 hours (preferably 4 hours), to afford the corresponding alpha-hydroxy acid of Formula 1A. As illustrated in Reaction Scheme V, when R^(a) of Formula 105 is a silyl protecting group, the hydrolysis conditions are also effective for deprotection to restore the phenolic hydroxyl group. Alternatively, for example when R^(a) is methoxymethylethyl, the deprotection and hydrolysis procedures described with reference to Reaction Scheme X, can be employed.

Preparation of Chiral Compounds of Formula 1A

One method of preparing chiral compounds of Formula 1A is shown below in Reaction Scheme VI. ##STR33## Preparation of Formula 109

As illustrated in Reaction Scheme VI, Step 1, an unsaturated aldehyde of Formula 106 is reduced and then converted to the corresponding compound of Formula 109 in which R^(b) is a leaving group (a sulfonate or halide, preferably a bromide).

An unsaturated aldehyde of Formula 106 is reacted with from 0.5 to 2 (preferably 1) molar equivalents of a reducing agent (such as sodium cyanoborohydride or preferably sodium borohydride) in an alcoholic solvent (such as ethanol, isopropanol or preferably methanol). The reaction takes place at 0° to 50° C. (preferably 25° C.) for 1 to 12 hours (preferably 2 hours) to give the corresponding allylic alcohol (not shown) which is used without isolation or further purification.

The allylic alcohol is reacted with from 1 to 1.5 (preferably 1.25) molar equivalents of a sulfonating agent (such as p-toluenesulfonyl chloride) and an organic base, or preferably reacted with a halogenating reagent (such as carbon tetrachloride/triphenylphosphine or preferably N-bromosuccinimide/triphenylphosphine) in an inert organic solvent (such as ether or preferably dichloromethane). The reaction takes place at a temperature of -40° to 40° C. (preferably -10° C.) for 1 to 12 hours (preferably 2 hours) to afford the corresponding compound of Formula 109.

Preparation of Formula 110

As illustrated in Reaction Scheme VI, Step 2, an allylic halide or sulfonate of Formula 109 is alkylated with a chiral 4-alkyl N-acyl oxazolidinone of Formula 109a to give the corresponding chiral substituted acyl oxazolidinone of Formula 110.

An alkali metal (preferably lithium) salt of a chiral 4-alkyl N-acyl oxazolidinone of Formula 109a (the alkyl group preferably being 4-isopropyl) by reaction of the N-acyl oxazolidinone with 1 to 1.25 (preferably 1.05) molar equivalents of an alkali metal hydride, hexamethyldisilazide or dialkylamide (preferably lithium diisopropylamide) in an inert organic solvent (such as ether or preferably tetrahydrofuran). The reaction takes place at -100° to -20° C. (preferably -80° C.) for 5 to 120 minutes (preferably 30 minutes). The solution of the salt (1 to 1.5, preferably 1.25 molar equivalents) is then added to a solution of an allylic compound of Formula 109 in the same solvent. The alkylation reaction takes place at -100° to 0° C. (preferably -80° C.) for 30 minutes to 6 hours (preferably 1 hour) to afford the corresponding chiral substituted acyl oxazolidinone of Formula 110.

Preparation of Chiral Formula 1A

As illustrated in Reaction Scheme VI, Step 3, a chiral substituted acyl oxazolidinone of Formula 110 is hydrolyzed to the corresponding chiral acid of Formula 1A. Use of an acyl oxazolidinone of Formula 109a having a 4-alkyl substituent of the opposite configuration in Reaction Scheme VI, Step 2, followed by hydrolysis as described in Step 3 results in the corresponding chiral acid where Z³ has the opposite configuration.

An acyl oxazolidinone of Formula 110 is reacted with from 1.25 to 3.5 (preferably 3.0) molar equivalents of lithium hydroxide, in a mixture of water and a water-miscible organic solvent (such as dioxane or preferably tetrahydrofuran) containing from 6 to 10 (preferably 8) molar equivalents of 30% aqueous hydrogen peroxide. The reaction takes place at -20° to 40° C. (preferably 20° C.) for 1 to 24 hours (preferably 12 hours) to afford the corresponding chiral acid of Formula IA.

Alternative Preparation of Compounds of Formula 1A

An alternative preparation of compounds of Formula 1A is shown below in Reaction Scheme VII. ##STR34## Preparation of Formula 112

As illustrated in Reaction Scheme VII, Step 1, an allylic compound of Formula 109 in which R^(b) is a leaving group (a sulfonate or halide, preferably a bromide) is condensed with an ester of Formula 109b to give the mono- or di-alkyl ester of Formula 112 (where Z³ is hydrogen, lower alkyl, lower alkenyl, or phenyl and Z⁴ is hydrogen, lower alkyl, or phenyl).

An ester of Formula 109b is converted to an alkali metal salt by reaction with 1.05 to 1.25 (preferably 1.1) molar equivalents of an alkali metal amide (such as sodium hexamethyldisilazide, potassium tetramethylpiperidide or preferably lithium diisopropylamide) in an organic solvent (such as ether, dioxane or preferably tetrahydrofuran). The reaction takes place at -40° to 30° C. (preferably 0° C.) for 15 minutes to 3 hours (preferably 30 minutes). Without isolation or further purification, the resulting solution of the alkali metal salt of the ester of Formula 109b (1.2 to 1.6, preferably about 1.3 molar equivalents) is then reacted with an allylic compound of Formula 109, in the same solvent, optionally in the presence of from 2% to 10% (preferably about 5%) by volume of hexamethyl phosphoric triamide. The reaction takes place at -100° to -40° C. (preferably -80° C.) for 30 minutes to 6 hours (preferably 1 hour) to afford the corresponding alkyl ester of Formula 112.

Preparation of Formula 1A

Compound of Formula 1A are then obtained as esters by deprotection of compounds of Formula 105 as described below with reference to Reaction Scheme X, Step 1; they are hydrolyzed to the corresponding carboxylic acid as described below with reference to Reaction Scheme X, Step 2.

Preparation of Compounds of Formula 1A where Z³ is S(O)_(m) alkyl

Compounds of Formula 1A where Z³ is S(O)_(m) alkyl are prepared as shown below in Reaction Scheme VIII. ##STR35## Preparation of Formula 1A where Z³ is S(O)_(m) alkyl

As illustrated in Reaction Scheme VIII, Step 1, a 2-(alkylthio)-4-hexenoic acid ester of Formula 1A (where Z³ is S-lower alkyl, and Z⁴ is hydrogen or lower alkyl) is oxidized to give the corresponding 2-(alkylsulfinyl)- or 2-(alkylsulfonyl)-4-hexenoic acid ester of Formula 1A where Z³ is S(O)lower alkyl or S(O)₂ lower alkyl. Alternatively, the reaction can be performed with an acid of Formula 1A where Z³ is S-lower alkyl, to give the corresponding acid where Z³ is 2-(alkylsulfinyl) or 2-(alkylsulfonyl).

An alkylthio-4-hexenoic acid ester of Formula 1A is reacted with 1.0 to 1.25 (preferably 1.05) molar equivalents of an oxidizing agent (such as oxone®) optionally in the presence of an inert support (such as alumina), in a solvent (such as chloroform or preferably dichloromethane). The reaction takes place at 0° to 55° C. (preferably 35° C.) for 1 to 10 hours (preferably 2 hours) to afford the corresponding 2-(alkylsulfinyl)-4-hexenoic acid ester of Formula 1A where Z³ is S(O)lower alkyl.

By repeating the foregoing procedure under the same conditions [starting with the 2-(alkylsulfinyl)-4-hexenoic acid ester so-produced], or by conducting the reaction with the 2-(alkylthio)-4-hexenoic acid ester starting material [and using 2.0 to 2.5 (preferably 2.25) molar equivalents of oxone] the corresponding 2-alkylsulfonyl-4-hexenoic acid esters are produced.

A 2-(alkylsulfinyl)- or 2-(alkylsulfonyl)-4-hexenoic acid ester of Formula I-ZA-K is hydrolyzed to give the corresponding acid as described with reference to Reaction Scheme X, Step 2.

Preparation of Compounds of Formula 1A where Z¹ is Halo

Compounds of Formula 1A where Z¹ is halo are prepared as shown below in Reaction Scheme IX. ##STR36## Preparation of Formula 114

As illustrated in Reaction Scheme IX, Step 1, a protected aldehyde of Formula 103 and a triphenylphosphoranylideneacetate of Formula 103c are combined in a Wittig reaction to give the corresponding alkyl-2-halo-butenoate ester of Formula 114.

An aldehyde of Formula 103 is reacted with 1.0 to 1.5 (preferably 1.1) molar equivalents of an alkyl 2-halo-2-triphenylphosphoranylideneacetate of Formula 103c (the halo group preferably being chloro) in an organic solvent (such as acetonitrile, or preferably toluene). The reaction takes place at 50° to 120° C. (preferably 110° C.) for 4 to 48 hours (preferably 24 hours) to afford the corresponding alkyl 2-halo-4-aryl-2-butenoate ester of Formula 114.

Preparation of Formula 115

As illustrated in Reaction Scheme IX, Step 2, a protected alkyl 2-halo-4-aryl-2-butenoate ester of Formula 114 is converted to the corresponding bromide of Formula 115 after reduction to the corresponding alcohol (not shown).

A 2-halo-4-aryl-2-butenoate ester of Formula 114 (preferably a t-butyl ester) is converted to the corresponding acid (preferably by dissolution in trifluoroacetic acid at room temperature for 1 to 2 hours). The acid is isolated and purified by conventional means, then reacted with 0.5 to 3 (preferably 1.6) molar equivalents of a reducing agent (such as sodium cyanoborohydride, sodium borohydride, or preferably borane dimethyl disulfide complex) in an inert solvent (such as methanol, ethanol, isopropanol or preferably THF). The reaction takes place at 0° to 50° C. (preferably 25° C.) for 1 to 48 hours (preferably 24 hours) to give the corresponding alcohol (not shown) which is used after purification.

The allylic alcohol so-produced is reacted with from 1 to 1.5 (preferably 1.25) molar equivalents of a sulfonating agent (such as p-toluenesulfonyl chloride) and an organic base, or preferably reacted with a halogenating reagent (such as carbon tetrachloride/triphenylphosphine or preferably N-bromosuccinimide/triphenylphosphine) in an inert organic solvent (such as ether or preferably dichloromethane). The reaction takes place at a temperature of -40° to 40° C. (preferably -10° C.) for 1 to 12 hours (preferably 2 hours) to afford the corresponding 2-halo-4-aryl-2-butenyl bromide compound of Formula 115.

Preparation of Formula 1A where Z¹ is Halo

As illustrated in Reaction Scheme IX, Step 3, a protected 2-halo-4-aryl-2-butenyl bromide compound of Formula 115 is condensed with a dialkyl malonate of Formula 116, substituted by Z⁴ (where Z⁴ is hydrogen, lower alkyl, or phenyl), which is hydrolysed and decarboxylated to give the corresponding 4-halo-4-hexenoic acid derivative of Formula 1A where Z¹ is halo.

An ester of Formula 116 (where Z⁴ is hydrogen, lower alkyl, or phenyl) is converted to an alkali metal salt by reaction with 1.05 to 1.25 (preferably 1.1) molar equivalents of an alkali metal hydride (preferably sodium hydride) in an organic solvent (such as ether, dioxane or preferably tetrahydrofuran). The reaction takes place at -40° to 30° C. (preferably 0° C.) for 15 minutes to 3 hours (preferably 30 minutes). Without isolation or further purification, the resulting solution of the alkali metal salt of the ester of Formula 106b (1.2 to 1.6, preferably about 1.3 molar equivalents) is then reacted with an allylic bromo compound of Formula 115 in the same solvent. The reaction takes place at -20° to 50° C. (preferably 25° C.) for 30 minutes to 6 hours (preferably 2 hours) to afford the corresponding dialkyl ester derivative.

The dialkyl ester thus produced is then hydrolysed conventionally, using a strong base, preferably aqueous sodium hydroxide, in a protic solvent, preferably ethanol, heating to reflux. The dicarboxylic acid thus produced is separated conventionally, and then decarboxylated by heating, preferably in a high-boiling inert solvent, most preferably 1,2-dichlorobenzene, to give the corresponding 4-halo-4-hexenoic acid derivative of Formula 1A where Z¹ is halo.

PREPARATION OF THE COMPOUNDS OF FORMULA 1A

Compounds of Formula 1A as esters and carboxylic acids are obtained by deprotection and hydrolysis as shown below in Reaction Scheme X. ##STR37## Preparation of Formula 1A as an Ester

As illustrated in Reaction Scheme X, Step 1, a protected phenol of Formula 117 (which can be any of the corresponding protected compounds of Reaction Schemes I to IX, such as Formulae 105, 107, 108, 112, and the like) is deprotected to give the corresponding alkyl ester of Formula 1A as an ester.

An alkyl ester of Formula 117 (having either an acetal-type or a silyl-type protecting group) is treated with from 0.05 to 0.2 molar equivalents (preferably 0.1 molar equivalents) of an aqueous mineral acid (such as sulfuric, perchloric, or preferably hydrochloric acid), in a water-miscible organic solvent (such as methanol, acetone, or preferably ethanol). The reaction takes place at 0° to 50° C. (preferably 25° C.) over a period of 1 to 6 hours (preferably 2 hours) to give the corresponding free phenol of Formula 1A.

Alternatively, to remove acetal-type protecting groups (such as MEM) a compound of Formula 117 is treated with 0.05 to 0.25 molar equivalents (preferably 0.1 molar equivalents) of a Lewis acid (such as zinc chloride or preferably zinc bromide), in a solvent (such as benzene, chloroform, or preferably dichloromethane). The reaction takes place at 0° to 50° C. (preferably 25° C.) over a period of 1 to 12 hours (preferably 3 hours) to give the corresponding free phenol of Formula 1A.

Alternatively, to remove silyl-type protecting groups (such as t-butyldimethylsilyl) a compound of Formula 117 is reacted with 1.0 to 1.5 (preferably 1.25) moles of a tetraalkyl ammonium fluoride (preferably tetrabutylammonium fluoride) in an ethereal solvent (such as dioxane or preferably tetrahydrofuran). The reaction takes place at -10° to 25° C. (preferably 0° C.) over a period of 0.1 to 2 hours (preferably 0.5 hours) to give the corresponding free phenol of Formula 1A.

Preparation of Formula 1A as a Carboxylic Acid

As illustrated in Reaction Scheme X, Step 2, a compound of Formula 1A as an ester (prepared as described above) is hydrolyzed to give the corresponding acid of Formula 1A as a carboxylic acid.

An alkyl ester of Formula 1A is reacted with from 1.5 to 4 molar equivalents (preferably 2 molar equivalents) of an inorganic hydroxide (such as potassium, sodium, or preferably lithium hydroxide) in a mixture of water and an organic solvent (such as tetrahydrofuran, methanol, or preferably dimethoxyethane). The reaction takes place at 0° to 60° C. (preferably 40° C.) over a period of 1 to 12 hours (preferably 3 hours). The resulting anion is acidified with an aqueous mineral acid (such as hydrochloric acid). The acidification takes place at 0° to 40° C. (preferably 25° C.) over a period of I to 10 minutes (preferably 2 minutes) to give the corresponding carboxylic acid of Formula 1A.

PREPARATION OF COMPOUNDS OF FORMULA 1A

One method of preparing compounds of Formula 1 where Z is a sidechain of Formula ZB, illustrated as compounds of Formula 1B, is shown below in Reaction Schemes XI and XII. ##STR38## where M is Li or MgBr ##STR39## Preparation of Formula 202

As illustrated in Reaction Scheme XI, Step 1, the aldehyde of Formula 103 is converted to a carbinol of Formula 202 by addition of an unsaturated cyclic organometallic compound of Formula 201 where M is Li or MgBr, prepared for example as described above with reference to Reaction Scheme I, Step 3.

One molar equivalent of the organometallic reagent 201 is added to a solution of an aldehyde of Formula 103 (in the same solvent system used to make the organometallic reagent). The reaction takes place at -80° to -20° C. (preferably -40° C.) over a period of 5 to 60 minutes (preferably 15 minutes) to give the corresponding carbinol of Formula 202.

Resolution of Formula 202

The racemic compound of Formula 202 may be separated into its two enantiomers by conventional means, for example by conversion into two diastereoisomers that are then separated by crystallization, chromatography, or by any conventional separation technique. Preferably, the carbinol is reacted with a chiral isocyanate to give a mixture of diastereoisomeric carbamates, which are separated by chromatography and cleaved to give the pure enantiomers.

A carbinol of Formula 202 is heated at 30° to 100° C. (preferably about 60° C.) with 2 to 6 molar equivalents (preferably 4 molar equivalents) of a chiral isocyanate in the presence of 1 to 1.5 molar equivalents (preferably 1.2 molar equivalents) of a strong organic base, for example 4-dimethylaminopyridine, in a hindered tertiary amine (for example diisopropylethylamine) as a solvent. The reaction takes place over a period of 1 to 24 hours (preferably 7 hours) to give the corresponding carbamate as a mixture of diastereoisomers.

The mixture of diastereoisomeric carbamates is separated by conventional means, preferably chromatography. The individual diastereoisomers are then separately cleaved by treatment with 1 to 1.5 molar equivalents (preferably 1.2 molar equivalents) of a trihalosilane, for example trichlorosilane, in the presence of an excess of a tertiary amine, for example triethylamine, in an inert solvent, for example toluene. The reaction takes place at a temperature of 90°-120° C. (preferably 110° C.) over a period of 5 minutes to 2 hours (preferably 15 minutes) to give the corresponding enantiomer of the carbinol of Formula 202.

Preparation of Formula 203

As illustrated in Reaction Scheme XI, Step 2, an alkyl ester of Formula 203 is formed by a Claisen ortho ester reaction of a carbinol of Formula 201 (or an enantiomer thereof) with an appropriately substituted orthoester.

A carbinol of Formula 202 is heated at 50° to 140° C. (preferably 130° C.) with a large excess of an orthoester of Formula 104a (see Reaction Scheme I, step 4), in the presence of from 0.05 to 0.25 molar equivalents (preferably 0.10 molar equivalents) of an organic acid catalyst (such as propionic, butyric, or trimethylacetic acid, preferably trimethylacetic acid). The reaction takes place over a period of 1 to 24 hours (preferably 2.5 hours) to give the corresponding alkyl ester of Formula 203.

Preparation of Formula 1B

Compounds of Formula 1B are prepared as described with reference to Reaction Scheme X, Step 1 (deprotection to afford the corresponding alkyl ester of Formula 1B), and Step 2 (hydrolysis to afford the corresponding acid of Formula 1B).

Alternative Preparation of Enantiomers of Compounds of Formula 1B

Another method of preparing individual enantiomers of compounds of Formula 1 where Z is sidechain ZB, illustrated as compounds of Formula 1B, is from chiral compounds of Formula 202b, the preparation of which is shown below in Reaction Scheme XII. ##STR40## Preparation of Formula 202a

Compounds of Formula 202a are prepared as described above with reference to Reaction Scheme II, Step 3 (conversion of 103g to 103h).

Preparation of Formula 202b

Compounds of Formula 202b are prepared as described above with reference to Reaction Scheme II, Step 4 (conversion of 103h to 104b).

Preparation of Enantiomers of Compounds of Formula 1B

The chiral carbinol of Formula 202b is then converted to an enantiomer of a compound of Formula 1B in the same manner as shown above in Reaction Scheme XI (conversion of compounds of Formula 202 to 203 to 1B).

Preparation of Compounds of Formula 1C

One method of preparing compounds of Formula 1 where Z is a sidechain of Formula ZC, illustrated as compounds of Formula 1C, is shown below in Reaction Scheme XIII. ##STR41## Preparation of Formula 302

As illustrated in Reaction Scheme XIII, Step 1, an aldehyde of Formula 103 (prepared, for example as described above with reference to Reaction Scheme I, Steps 1 and 2) is transformed into an unsaturated aldehyde of Formula 302 by a Wittig reaction with an ylid of Formula 301 (where Z⁵ is hydrogen or lower alkyl).

An aldehyde of Formula 103 is reacted with one molar equivalent of an ylid of Formula 301, in an organic solvent (such as dichloromethane, dimethylformamide or preferably toluene). The reaction takes place at 0° to 110° C. (preferably 80° C.) for 1 to 24 hours (preferably 8 hours) to give the corresponding unsaturated aldehyde of Formula 302.

Preparation of Formula 303

As illustrated in Reaction Scheme XIII, Step 2, an unsaturated aldehyde of Formula 302 is converted to the corresponding vinyl carbinol of Formula 303.

An aldehyde of Formula 302 is reacted with from 1.0 to 1.25 (preferably 1.1) molar equivalents of an organovinyl compound (preferably vinylmagnesium bromide) in a solvent (such as ether or preferably tetrahydrofuran). The reaction takes place at -30° to 20° C. (preferably at 0° C.) for 0.1 to 4 hours (preferably 0.5 hours) to give the corresponding vinyl carbinol of Formula 303.

Preparation of Formula 304

As illustrated in Reaction Scheme XIII, Step 3, a vinyl carbinol of Formula 303 is oxidized to give the corresponding dienone of Formula 304.

A vinyl carbinol of Formula 303 is reacted with 1.0 to 1.5 (preferably 1.1) molar equivalents of an oxidizing agent (such as manganese dioxide, pyridinium chlorochromate or preferably pyridinium dichromate) in a solvent (such as pyridine or preferably dichloromethane). The reaction takes place at 0° to 30° C. (preferably 25° C.) for 30 minutes to 4 hours (preferably 1 hour) to give the corresponding dienone of Formula 304.

Preparation of Formula 305

As illustrated in Reaction Scheme XIII, Step 4, a dienone of Formula 304 is cyclized to give the corresponding cyclopentenone of Formula 305.

A dienone of Formula 304 reacted with 0.3 to 1.5 (preferably 1.0) molar equivalents of a Lewis acid (such as boron trichloride, tin (IV) chloride or preferably boron trifluoride etherate) in a solvent (such as tetrachloroethane or preferably dichloromethane). The reaction takes place at 0° to 30° C. (preferably 25° C.) for 1 to 6 hours (preferably 2 hours) to give the corresponding cyclopentenone of Formula 305.

Preparation of Formula 306

As illustrated in Reaction Scheme XIII, Step 5, a cyclopentenone of Formula 305 is reduced to give the corresponding cyclopentenol of Formula 306.

A cyclopentenone of Formula 305 is reacted with 1.0 to 1.5 (preferably 1.1) molar equivalents of a reducing agent (such as lithium tri-tert-butoxyaluminium hydride or preferably sodium borohydride in the presence of an equimolar amount of cerium trichloride) in a mixture of an ethereal solvent (preferably tetrahydrofuran) and a lower alkanol (preferably methanol). The reaction takes place at 0° to 40° C. (preferably at 25° C.) for 1 to 6 hours (preferably 2 hours) to give the cyclopentenol of Formula 306.

Preparation of Formula 307

As illustrated in Reaction Scheme XIII, Step 6, a cyclopentenol of Formula 306 is transformed to the corresponding vinyl ether of Formula 307.

A cyclopentenol of Formula 306 is reacted with from 10 to 100 (preferably 50) molar equivalents of a 1-alkenyl ether, optionally in the presence of a co-solvent (such as ether or tetrahydrofuran), in the presence of from 0.1 to 0.5 (preferably 0.3) molar equivalents of a mercury (II) salt (preferably mercury (II) acetate). The reaction takes place at 0° to 50° C. (preferably 25° C.) for 1 to 5 days (preferably 2 days) to give the corresponding vinyl ether of Formula 307.

Preparation of Formula 308

As illustrated in Reaction Scheme XIII, Step 7, a vinyl ether of Formula 307 is rearranged to the corresponding acetaldehyde of Formula 308.

A vinyl ether of Formula 307 is reacted with from 10 to 100 (preferably 50) molar equivalents of a lithium salt (such as the tetrafluoroborate or preferably the perchlorate) in a solvent (such as tetrahydrofuran or preferably ether). The reaction takes place at 0° to 35° C. (preferably 25° C.) for 0.1 to 2 hours (preferably 0.5 hours) to give the corresponding acetaldehyde of Formula 308.

Preparation of Formula 309

As illustrated in Reaction Scheme XIII, Step 8, an acetaldehyde of Formula 308 is oxidized to give the corresponding acid of Formula 309.

An acetaldehyde of Formula 308 is reacted with 1 to 3 (preferably 1.5) molar equivalents of a suitable oxidizing agent (such as silver oxide, Jones reagent or preferably sodium chlorite) in the presence of an equimolar amount of a phenol (such as quinol or preferably resorcinol). The reaction is conducted in a mixture of water and a water-miscible organic solvent (such as tetrahydrofuran or preferably dioxane) at a pH of from 4 to 6 (preferably 5) at -10° to 25° C. (preferably 0° C.) for 10 minutes to 2 hours (preferably 30 minutes) to give the corresponding acid of Formula 309.

Preparation of Formula 1C

As illustrated in Reaction Scheme XIII, Step 9, an acid of Formula 309 is deprotected to give the corresponding acid of Formula 1C.

An acid of Formula 309 where R^(a) is a sulphonyloxy protecting group hydrolyzed under basic conditions, using from 1 to 5 (preferably 3) molar equivalents of an alkali metal hydroxide (preferably lithium hydroxide) in a mixture of water and a water-miscible organic solvent (such as dioxane or preferably methanol). The reaction takes place at 40° to 100° C. (preferably 60° C.) for 1 to 48 hours (preferably 12 hours) to afford the corresponding cyclopentene carboxylic acid of Formula 1C.

Alternatively, for other protecting groups, the deprotection reaction takes place as described above with reference to Reaction Scheme X, Step 1.

PREPARATION OF COMPOUNDS OF FORMULA 1D

One method of preparing compounds of Formula 1 where Z is a sidechain of Formula ZD, illustrated as compounds of Formula 1D, is shown below in Reaction Scheme XIV. ##STR42## Preparation of Formula 401

As illustrated in Reaction Scheme XIV, Step 1, an aldehyde of Formula 103 (where R^(a) is a silyl protecting group) is converted to a carbinol by addition of an organometallic compound of Formula 103d (such as a substituted vinyl organolithium, or preferably a Grignard reagent where: M is MgBr or Li; Z² is hydrogen or lower alkyl; and TBS is a tert-butyldimethylsilyl protecting group).

The aldehyde of Formula 103 is reacted with from 1.1 to 1.5 (preferably 1.25) molar equivalents of an organometallic, preferably organolithium, derivative of a protected 2-halo (preferably 2-bromo) but-1-en-4-ol. The reaction is performed at from -100° to -40° C. (preferably at -78° C.) for from 30 minutes to 6 hours (preferably 1 hour) to afford the corresponding compound of Formula 401.

Preparation of Formula 402

As illustrated in Reaction Scheme XIV, Step 2, an alkyl ester of Formula 402 is formed by a Claisen ortho ester rearrangement reaction of a carbinol of Formula 401 and a trialkyl orthoacetate of Formula 104a.

A carbinol of Formula 401 is heated at 50° to 120° C. (preferably about 100° C.) with about 10 molar equivalents of an orthoester of Formula 104a, in the presence of from 0.05 to 0.25 (preferably 0.10) molar equivalents of an organic acid catalyst (such as propionic, butyric, or preferably trimethylacetic acid). The reaction takes place over a period of 1 to 48 hours (preferably 8 hours) to give the corresponding alkyl ester of Formula 402.

Preparation of Formula 403

As illustrated in Reaction Scheme XIV, Step 3, an alkyl ester of Formula 402 is reacted with a tetraalkylammonium fluoride and then halogenated to give a protected ester of Formula 403.

A compound of Formula 402 is reacted with from 2 to 3 (preferably 2) molar equivalents of a tetraalkylammonium (preferably tetrabutylammonium) fluoride, in a solvent (such as dioxane or preferably methylene chloride) at from 0° to 25° C. (preferably 10° C.), for from 30 minutes to 4 hours (preferably 1 hour). The product so obtained is reacted with from 1.0 to 1.5 (preferably 1.25) molar equivalents of a halogenating agent (preferably a brominating agent, such as triphenylphosphine/carbon tetrabromide or preferably triphenylphosphine/N-bromosuccinimide) in a solvent such as ether or preferably dichloromethane. The reaction takes place at from -40° to 0° C. (preferably -10° C.) for from 1 to 6 hours (preferably 4 hours) to give the corresponding halogenated ester of Formula 403.

Preparation of Formula 1D

As illustrated in Reaction Scheme XIV, Step 4, a halogenated ester of Formula 403 is cyclized to give a cycloalkyl ester of Formula 1C.

A compound of Formula 403 is reacted with from 2.0 to 2.5 (preferably 2.25) molar equivalents of a strong base (such as lithium diisopropylamide, sodium hydride or preferably sodium hexamethyldisilazide) in an ethereal solvent (such as ether, dioxane or preferably tetrahydrofuran) The reaction takes place at from -100° to -60° C. (preferably -78° C.) for 1 to 12 hours (preferably 4 hours) to give the cycloalkyl ester of Formula 1D, which may be hydrolyzed to the carboxylic acid of Formula 1D as described above with reference to Reaction Scheme X, Step 2.

PREPARATION OF COMPOUNDS OF FORMULA 1E

Methods of preparing compounds of Formula 1 where Z is sidechain of Formula ZE, illustrated as compounds of Formula 1E, is shown below in Reaction Schemes XV to XVII. ##STR43## Preparation of Formula 502

As illustrated in Reaction Scheme XV, Step 1, the 2-methyl group of an alkyl 2-methylbenzoate of Formula 501 (where Z⁶ and Z⁷ are selected from hydrogen, lower alkyl, lower alkoxy, lower alkoxycarbonyl, halo and nitro) is brominated to give the corresponding compound of Formula 502.

An ester of Formula 501 is reacted with 1.0 to 1.2 (preferably 1.05) molar equivalents of a brominating agent (such as N-bromoacetamide or preferably N-bromosuccinimide), optionally in the presence of an initiator (such as visible light) or from 0.001 to 0.01 (preferably 0.005) molar equivalents of a chemical initiator (such as azobisisobutyronitrile or preferably benzoyl peroxide) in a solvent (such as ethyl formate or preferably carbon tetrachloride). The reaction takes place at 40° to 80° C. (preferably 75° C.) for 30 minutes to to 6 hours (preferably 2 hours) to afford the corresponding alkyl 2-bromomethylbenzoate of Formula 502, which can be purified by conventional means or preferably used directly for the next step.

Preparation of Formula 503

As illustrated in Reaction Scheme XV, Step 2, a 2-bromomethyl group of Formula 502 is converted to the corresponding phosphonium salt of Formula 503.

A 2-bromomethylbenzoate of Formula 502 is reacted with 1.0 to 1.25 (preferably 1.05) molar equivalents of a triaryl phosphine (preferably triphenyl phosphine) in a solvent (such as dimethylformamide or preferably acetonitrile). The reaction takes place at 25° to 90° C. (preferably 50° C.) for 1 to 24 hours (preferably 2 hours) to afford the corresponding phosphonium salt of Formula 503.

Preparation of Formula 504

As illustrated in Reaction Scheme XV, Step 3, a phosphonium salt of Formula 503 is converted to the corresponding substituted benzylidenetriphenylphosphorane ylid of Formula 504.

A phosphonium salt of Formula 503 is dissolved or suspended in a solvent (such as dioxane, ether or preferably dimethylformamide) and reacted with 1.0 to 1.25 (preferably 1.05) molar equivalents of a base (such as sodium hydride, triethylamine or preferably 1,5-diazabicyclo[4.3.0]non-5-ene). The reaction takes place at 0° to 60° C. (preferably 25° C.) for 1 to 6 hours (preferably 2 hours) to afford the corresponding ylid of Formula 504, which can be isolated by conventional means or its solution can be used directly for the next step.

Preparation of Formulae 505 and 506

As illustrated in Reaction Scheme XV, Step 4, an ylid of Formula 504 and a protected aldehyde of Formula 103 (prepared, for example, as described in connection with Reaction Scheme ZA-A, Step 2) are employed in a Wittig reaction to give the corresponding protected substituted benzoic acid alkyl ester of Formula 505 as a mixture of E and Z isomers, from which the desired E isomer of Formula 506 is isolated, as illustrated in Reaction Scheme XV, Step 5.

A solution of 0.8 to 1.0 (preferably 0.95) molar equivalents of a protected aldehyde of Formula 103 in a solvent (such as ether, dioxane or preferably dimethylformamide) is added to a solution of an ylid of Formula 504 in the same solvent. The reaction takes place at 0° to 50° C. (preferably 25° C.) for 1 to 24 hours (preferably 12 hours) to afford the corresponding protected substituted benzoic acid alkyl ester of Formula 505 as a mixture of E and Z isomers, from which the desired E-isomer of Formula 506 can be isolated by conventional means (such as distillation, chromatography or preferably fractional crystallization). ##STR44## Preparation of Formula 508

As illustrated in Reaction Scheme XVI, Step 1, the alpha carbon of an alkyl 2-alkylbenzoate of Formula 507 (where Z⁵ is hydrogen or lower alkyl, and Z⁶ and Z⁷ are selected from hydrogen, lower alkyl, lower alkoxy, lower alkoxycarbonyl, halo and nitro) is brominated to give the corresponding compound of Formula 508. The reaction takes place under the conditions described with reference to Reaction Scheme XV, Step 1.

Preparation of Formula 509

As illustrated in Reaction Scheme XVI, Step 2, an alkyl 2-bromo-alkylbenzoate of Formula 508 and a trialkyl phosphite are combined in an Arbuzov reaction to give the corresponding phosphonate of Formula 509.

A compound of Formula 508 is reacted with from 5 to 20 (preferably 10) molar equivalents of a trialkyl phosphite (preferably triethyl phosphite). The reaction takes place at 100° to 200° C. (preferably 150° C.) for 1 to 24 hours (preferably 6 hours) to afford the corresponding phosphonate of Formula 509.

Preparation of Formulae 510 and 511

As illustrated in Reaction Scheme XVI, Step 3, a phosphonate of Formula 509 and a protected aldehyde of Formula 103 (prepared, for example, as described in connection with Reaction Scheme I, Step 2) are reacted to give the corresponding protected substituted benzoic acid alkyl ester of Formula 510 as a mixture of E and Z isomers, from which the desired E isomer of Formula 511 is isolated, as illustrated in Reaction Scheme XV, Step 4.

A phosphonate of Formula 509 is reacted with 1.0 to 1.5 (preferably 1.1) molar equivalents of a base such (as sodium amide, potassium tert-butoxide or preferably sodium hydride) for from 1 to 4 hours (preferably 2 hours) at 0° to 50° C. (preferably 25° C.) in a solvent (such as dioxane, dimethylformamide or preferably dimethoxyethane), to give a solution or suspension of the corresponding alkali metal salt of Formula 509, which is employed without isolation or further purification. The alkali metal salt is reacted with from 0.9 to 1.1 (preferably 1.0) molar equivalents of a protected aldehyde of Formula 103, dissolved in the same solvent. The reaction takes place at 0° to 60° C. (preferably 40° C.) for 1 to 6 hours (preferably 2 hours) to afford the corresponding protected optionally substituted benzoic acid alkyl ester of Formula 510 as a mixture of E and Z isomers, from which the desired E-isomer of Formula 511 can be isolated by conventional means (such as distillation, chromatography or preferably fractional crystallization). ##STR45## Preparation of Formula 513

As illustrated in Reaction Scheme XVII, Step 1, a protected aldehyde of Formula 103 is converted to a trialkylsilylcarbinol of Formula 513 in a Grignard reaction.

An aldehyde of Formula 103 is reacted with from 1.0 to 1.25 (preferably 1.1) molar equivalents of a trialkylsilylalkyl-magnesium bromide (such as trimethylsilylpropylmagnesium bromide, or preferably trimethylsilylmethylmagnesium bromide) of Formula 512, in an ethereal solvent (such as ether, dimethoxyethane or preferably tetrahydrofuran). The reaction takes place at -40° to 40° C. (preferably 0° C.) for 30 minutes to 4 hours (preferably 1 hour) to give the corresponding trialkylsilylcarbinol of Formula 513.

Preparation of Formula 514

As illustrated in Reaction Scheme XVII, Step 2, a protected trialkylsilylcarbinol of Formula 513 is dehydrated to give the corresponding protected alkene as a mixture of E and Z isomers, from which the desired Z isomer of Formula 514 is isolated.

A carbinol of Formula 513 is reacted with from 1.0 to 1.5 (preferably 1.05) molar equivalents of a sulphonyl chloride (such as p-toluenesulphonyl chloride or preferably methanesulphonyl chloride) in the presence of the same molar proportion of a tertiary organic base (such as N-methylpyrrolidine or preferably triethylamine). The reaction takes place at 0° to 40° C. (preferably 15° C.) for 30 minutes to 4 hours (preferably 2 hours) to afford the corresponding protected alkene of Formula 514 as a mixture of E and Z isomers, from which the desired Z-isomer of Formula 514 can be isolated by conventional means (such as distillation, chromatography or preferably fractional crystallization).

Preparation of Formula 515

As illustrated in Reaction Scheme XVII, Step 3, an alkene of Formula 514 where R^(a) is a silyl protecting group is converted to an alkene of Formula 515 where R^(a) is an acyl group.

An alkene of Formula 514 is heated at 50°-130° C. (preferably about 118° C.) with a large excess of a mixture (preferably about equimolar) of a carboxylic acid of Formula R^(a) OH and an anhydride of Formula (R^(a))₂ O(where R^(a) is the desired acyl group), preferably a mixture of acetic acid and acetic anhydride. The reaction takes place over a period of 6 to 48 hours (preferably 18 hours) to give the corresponding alkene of Formula 515 where R^(a) is the acyl group.

Preparation of Formula 511

As illustrated in Reaction Scheme XVII, Step 4, a protected alkene of Formula 515 is converted to a protected optionally substituted benzoic acid alkyl ester of Formula 511 in a Heck reaction with an alkyl-2-halo-benzoate of Formula 515.

An alkene of Formula 515 is reacted with 1.0 to 2.0 (preferably 1.25) molar equivalents of an alkyl 2-halobenzoate (such as an alkyl 2-bromobenzoate or preferably 2-iodobenzoate). The reaction is conducted in the presence of from 0.001 to 0.1 (preferably 0.05) molar equivalents of a palladium catalyst [such as tetrakis(tri-o-tolylphosphine) palladium, or tetrakis(triphenylphosphine)palladium or preferably palladium (II) acetate] optionally in the presence of from 1.0 to 1.25 (preferably 1.05) molar equivalents of a base (such silver carbonate, sodium bicarbonate or preferably triethylamine), in a solvent (such as acetonitrile or preferably dimethylformamide). The reaction is conducted at from 0° to 120° C. (preferably 60° C.) for 1 to 48 hours (preferably 6 hours) to yield the corresponding protected optionally substituted benzoic acid alkyl ester of Formula 511.

Preparation of Formula 1E

The protected optionally substituted benzoic acid ester of Formula 506 or Formula 511 are then deprotected to give the corresponding ester of Formula 1E. The deprotection reaction takes place as described above with reference to Reaction Scheme X, Step 1. The optionally substituted benzoic acid ester of Formula 1E may then be hydrolyzed to give the corresponding acid of Formula 1E as described above with reference to Reaction Scheme X, Step 2.

PREPARATION OF FORMULA 1E where Z⁶ is Amino

The compounds of Formula 1E where Z⁶ is nitro are employed as precursors to the corresponding compounds of Formula 1E where Z⁶ is amino. The nitro compounds are also active as IMPDH inhibitors when tested as described below.

A nitrobenzoic acid of Formula 1E (where Z⁶ is nitro) is reacted with 1.0 to 3.0 (preferably 2.0) molar proportions of a reducing agent (such as sodium hydrosulfite or preferably tin (II) chloride) in hydrochloric acid solution, optionally in the presence of a water-miscible co-solvent (such as methanol or preferably acetic acid). The reaction takes place at 25° to 100° C. (preferably 75° C.) for 1 to 24 hours (preferably 4 hours) to afford the corresponding amino-substituted benzoic acid of Formula 1E (where Z⁶ is amino). ##STR46## Preparation of Formula 517

As illustrated in Reaction Scheme XVIII, Step 1, a phosphonate of Formula 509 undergoes a base catalyzed condensation (e.g., using 1 molar equivalent of sodium hydride) with tetrahydropyranyloxyacetaldehyde, in a solvent such as dimethylformamide. The reaction takes place at 25° C. over a period of 1 to 4 hours, to give E/Z mixture from which the desired product of Formula 517 can be isolated by conventional means, such as chromatography.

Preparation of Formula 518

As illustrated in Reaction Scheme XVIII, Step 2, the tetrahydropyranyloxy group of a compound of Formula 517 is hydrolyzed in the presence of a catalytic amount of a dilute acid (e.g., HCl) in aqueous tetrahydrofuran. The reaction takes place at 25° C. over a period of 1 to 4 hours, to give the corresponding carbinol of Formula 518.

Preparation of Formula 519

As illustrated in Reaction Scheme XVIII, Step 3, a carbinol of Formula 518 is converted to the halo (e.g., chloro or bromo) derivative of Formula 519 using 1 molar equivalent of triphenylphosphine and either carbon tetrachloride or carbon tetrabromide, in dichloromethane. The reaction takes place at 25° C. over a period of 2 hours.

Preparation of Formula 520

As illustrated in Reaction Scheme XVIII, Step 4, a halo derivative of Formula 519 undergoes a base-catalyzed ether formation with the indicated phenol, using 5 molar equivalents of potassium carbonate, in dimethylformamide. The reaction takes place at 25° C. over a period of 4 hours.

Preparation of Formula 1E

As illustrated in Reaction Scheme XVIII, Step 5, an ether of Formula 520 is rearranged to give the corresponding ester of Formula 1E by a thermal rearrangement catalysed by florisil. The rearrangement takes place in toluene at 110° C. over a period of one to four days.

As illustrated in Reaction Scheme XVIII, Step 6, the ether so-produced is hydrolyzed to the corresponding acid of Formula 1E as described with reference to Reaction Scheme X, Step 2.

PREPARATION OF COMPOUNDS OF FORMULA 1F

One method of preparing compounds of Formula 1 where Z is a sidechain of Formula ZF, illustrated as compounds of Formula 1F, is shown below in Reaction Scheme XIX. ##STR47## Preparation of Formula 602

As illustrated in Reaction Scheme XIX, Step 1, an aldehyde of Formula 601, prepared for example as shown in J. Org. Chem., 1977, p3408, is reduced to a carbinol of Formula 602.

An aldehyde of Formula 601 is reacted with a reducing agent capable of selectively reducing an aldehyde in the presence of ester groups, preferably from 1 to 2 (preferably 1.5) molar equivalents of sodium borohydride in the presence of from 1 to 2 (preferably 1.5) molar equivalents of cerium chloride trihydrate, in an alcoholic/ethereal solvent mixture (preferably 4:1 tetrahydrofuran:methanol). The reaction takes place at 0° to 40° C. (preferably 25° C.) for 10 minutes to 2 hours (preferably 30 minutes) to give the corresponding carbinol of Formula 602.

Preparation of Formula 604

As illustrated in Reaction Scheme XIX, Step 2, a phenol of Formula 603 is alkylated with a carbinol of Formula 602 by means of the Mitsonobu reaction to give an ether of Formula 604.

A carbinol of Formula 602 is reacted with an equimolar amount of a phenol of Formula 603 in the presence of from 1 to 3 (preferably 2) molar equivalents of a triarylphosphine, preferably triphenylphosphine, plus from 1 to 3 (preferably 1.5) molar equivalents of diethyl azodicarboxylate in an ethereal solvent (preferably tetrahydrofuran). The reaction takes place at 0° to 40° C. (preferably 25° C.) for 1 to 10 hours (preferably 3 hours) to give the corresponding ether of Formula 604.

Preparation of Formula 605

As illustrated in Reaction Scheme XIX, Step 3, a phenol of Formula 604 is thermally rearranged to give a diester of Formula 605.

An ether of Formula 604 is heated in an inert solvent (preferably toluene) in the presence of about 10 parts by weight of an activated magnesium silicate, preferably Florisil©. The reaction takes place at reflux temperature for 1 to 10 days (preferably 4 days) to give the corresponding diester of Formula 605.

Preparation of Formula 606

As illustrated in Reaction Scheme XIX, Step 4, a diester of Formula 605 is hydrolyzed to give a dicarboxylic acid of Formula 606.

A diester of Formula 605 is reacted with an excess of an inorganic base, preferably about 50 molar equivalents of lithium hydroxide, in an aqueous solvent (preferably 5:1 methanol:water). The reaction takes place at 0° to 40° C. (preferably 25° C.) for 1 to 10 days (preferably 2 days) to give the corresponding dicarboxylic acid of Formula 606.

Preparation of Formula 1F

As illustrated in Reaction Scheme XIX, Step 5, a dicarboxylic acid of Formula 606 is decarboxylated to give a monocarboxylic acid of Formula 1F.

A dicarboxylic acid of Formula 606 is heated (optionally in the presence of a high boiling inert solvent, for example tetramethylbenzene, but preferably in the absence of any solvent). The reaction takes place at 160° to 240° C. (preferably 195° C.) for about 5 minutes to give the corresponding monocarboxylic acid of Formula 1F.

PREPARATION OF COMPOUNDS OF FORMULA 1G

One method of preparing compounds of Formula 1 where Z is sidechain of Formula ZG, illustrated as compounds of Formula 1G, is shown below in Reaction Scheme XX. ##STR48## Preparation of Formula 703

As illustrated in Reaction Scheme XX, Step 1, the phenol of Formula 701 is alkylated with 3-hydroxycyclohexene to give the corresponding ether of Formula 703, by means of the Mitsonobu reaction. The Mitsonobu reaction takes place as described with reference to Reaction Scheme XIX, Step 2.

Similarly, by substituting 3-cyclohexene with 3-cycloheptene, and carrying out the procedures of Reaction Scheme XX, the corresponding compounds where Z is a side chain of Formula ZG where D³ is --CH₂ --CH₂ -- are obtained.

Preparation of Formula 704

As illustrated in Reaction Scheme XX, Step 2, a Claisen rearrangement of the ether of Formula 703 gives the alkylated phenol of Formula 704. The reaction takes place, e.g., at 200° C. for 12 to 16 hours in the presence of N,N-diethylaniline.

Preparation of Formula 705

As illustrated in Reaction Scheme XX, Step 3, the alkylated phenol of Formula 704 is protected to give a protected phenol of Formula 705 (where R^(a) is silyl or tosyl).

An alkylated phenol of Formula 704 is reacted with an equimolar amount of t-butyl dimethylsilyl chloride or p-toluenesulfonyl chloride, in the presence of an equimolar amount, respectively, of imidazole or 4-dimethylaminopyridine. The reaction takes place in dichloromethane at a temperature of 25° C. for 1 to 4 hours to give the corresponding protected phenol of Formula 705.

Preparation of Formula 706

As illustrated in Reaction Scheme XX, Step 4, a protected phenol of Formula 705 is converted to the corresponding dialdehyde of Formula 706 by ozonolysis. The ozonolysis reaction takes place as described with reference to Reaction Scheme I, Step 2.

Preparation of Formula 707

As illustrated in Reaction Scheme XX, Step 5, an intramolecular base-catalyzed aldol reaction with a dialdehyde of Formula 706 produces the corresponding formyl cyclopentene of Formula 707. The reaction is conducted with 0.1 moles of dibenzylamine or n-methylaniline trifluoroacetate in benzene, taking place at 50° C. for 30 minutes.

Preparation of Formula 708

As illustrated in Reaction Scheme XX, Step 6, a formyl cyclopentene of Formula 707 is reduced to the corresponding carbinol. The reaction employs sodium borohydride/cerium chloride, as described with reference to Reaction Scheme XIX, Step 1.

Preparation of Formula 709

As illustrated in Reaction Scheme XX, Step 7, a carbinol of Formula 708 is converted to the corresponding acetate of Formula 709. The reaction is conducted with equimolar amounts of acetyl chloride and triethylamine, taking place in methylene chloride at 0° C. for 1 hour.

Preparation of Formula 710

As illustrated in Reaction Scheme XX, Step 8, an acetate of Formula 709 is converted to the corresponding diester of Formula 710. The reaction is conducted as described in J. Am. Chem. Soc., 102:4730 (1980), with 4 moles of sodium dimethylmalonate, 0.5 moles triphenylphosphine and 0.25 moles of tetrakis triphenylphosphine palladium at 50° C. in tetrahydrofuran.

Preparation of Formula 711

As illustrated in Reaction Scheme XX, Step 9, an diester of Formula 710 is converted to the corresponding ester of Formula 711, by reaction with cesium acetate in hexamethylphosphoric triamide at 120° C. for 1 to 3 hours.

Preparation of Formula 1G

As illustrated in Reaction Scheme XX, Step 10, an ester of Formula 711 is hydrolyzed to give the corresponding compound of Formula 1G. The reaction takes place as described with reference to Reaction Scheme X, Step 2.

PREPARATION OF COMPOUNDS OF FORMULA 1H

One method of preparing compounds of Formula 1 where Z is sidechain of Formula ZH, illustrated as compounds of Formula 1H, is shown below in Reaction Scheme XXI. ##STR49## Preparation of Formula 801

As illustrated in Reaction Scheme XXI, Step 1, an aldehyde of Formula 103 is converted to a carbinol by addition of an organometallic compound of Formula 103e (such as a substituted vinyl organolithium, or preferably a Grignard reagent, where M is MgBr; TBS is a tert-butyldimethylsilyl protecting group; and n is 3-5).

A halovinyl (preferably bromovinyl) compound of Formula 103e (where M is halo) is reacted with magnesium metal in an ethereal solvent (such as ether or preferably tetrahydrofuran). The reaction takes place at 30° to 60° C (preferably 40° C.) over a period of 1 to 6 hours (preferably 2 hours). One molar equivalent of the resultant organometallic reagent is added to a solution of an aldehyde of Formula 103 (in the same solvent system used to make the organometallic reagent). The reaction takes place at -80° to 20° C. (preferably 0° C.) over a period of 5 to 60 minutes (preferably 10 minutes) to give the corresponding silyl-protected carbinol of Formula 801.

Preparation of Formula 802

As illustrated in Reaction Scheme XXI, Step 2, an alkyl ester of Formula 802 is formed by a Claisen ortho ester rearrangement reaction of a carbinol of Formula 801 and an orthoester compound of Formula 104a (as illustrated in Reaction Scheme I, where Z³ and Z⁴ are hydrogen).

A silyl-protected carbinol of Formula 801 is heated at 50° to 120° C. (preferably about 100° C.) with about 10 molar equivalents of an orthoester of Formula 104a, in the presence of from 0.05 to 0.25 molar equivalents (preferably 0.10 molar equivalents) of an organic acid catalyst (such as propionic, butyric, or preferably trimethylacetic acid). The reaction takes place over a period of 1 to 48 hours (preferably 8 hours) to give the corresponding alkyl ester of Formula 802.

Preparation of Formula 803

As illustrated in Reaction Scheme XXI, Step 3, the silyl-protected carbinol of an alkyl ester of Formula 802 is deprotected.

A compound of Formula 803 is reacted with from 5 to 30 (preferably 20) molar equivalents of hydrogen fluoride, in a mixture of water and a water-miscible organic solvent (preferably acetonitrile). The reaction takes place at -20° to 40° C. (preferably 25° C.) for 5 to 60 minutes (preferably 30 minutes) to afford the corresponding unprotected carbinol/alkyl ester of Formula 803.

Preparation of Formula 804

As illustrated in Reaction Scheme XXI, Step 4, a carbinol of Formula 803 is converted to a halide (preferably a bromide) of Formula 804, by means of a one-step or a two-step procedure.

In the one-step procedure, a carbinol of Formula 803 is reacted with from 1.0 to 1.3 (preferably 1.1) molar equivalents of a triaryl (preferably triphenyl) phosphine, and from 1.0 to 1.3 (preferably 1.1) molar equivalents of a halogen source (such as N-bromosuccinimide or preferably carbon tetrabromide). The reaction is conducted in an inert solvent (such as ether or preferably tetrahydrofuran). The reaction takes place at 0° to 50° C (preferably 25° C.) for 1 to 12 hours (preferably 3 hours) to afford the corresponding halide of Formula 804.

Alternatively, in the two-step procedure, which is preferred, a carbinol of Formula 803 is converted first into a sulphonate ester (such as a p-toluenesulphonate or preferably a methanesulphonate) by reaction with from 1.0 to 1.5 (preferably 1.3) molar equivalents a sulphonyl halide (preferably methanesulphonyl chloride) in the presence of an equimolar amount of a tertiary organic base (preferably diisopropylethylamine) in a solvent (such as chloroform or preferably dichloromethane). The reaction takes place at -20° to 30° C. (preferably 0° C.) for 10 to 60 minutes (preferably 30 minutes). The so-obtained sulphonate ester is then reacted with from 5 to 20 (preferably 20) molar equivalents of an alkali metal halide (preferably lithium bromide) in a solvent (such as 2-butanone or preferably acetone). The reaction takes place at 0° to 56° C. (preferably at reflux) for 30 to 180 minutes (preferably 90 minutes) to afford the corresponding halide of Formula 804.

Preparation of Formula 805

As illustrated in Reaction Scheme XXI, Step 5, a halogenated carbinol/alkyl ester of Formula 804 is deprotected at the phenolic group to give the corresponding halogenated carbinol/alkyl ester of Formula 805. The deprotection reaction takes place as described above with reference to Reaction Scheme X, Step 1.

Preparation of Formula 1H

As illustrated in Reaction Scheme XXI, Step 6, a halogenated carbinol/alkyl ester of Formula 805 is subjected to a base-induced cyclization reaction to afford the product of Formula 1H.

A compound of Formula 805 is reacted with from 2.0 to 2.5 (preferably 2.3) molar equivalents of a strong base (such as lithium diisopropylamide, sodium hydride or preferably sodium hexamethyldisilazide) in a solvent (such as dioxane or preferably tetrahydrofuran). The reaction takes place at -20° to 30° C. (preferably at 0° C.) for 5 to 60 minutes (preferably 15 minutes) to afford the corresponding cycloalkylester of Formula 1H. The cycloalkyl ester of Formula I-ZH-A1 may then be hydrolyzed to give the corresponding acid of Formula 1H. The hydrolysis takes place as described above with reference to Reaction Scheme X, Step 2.

Compounds of Formula 1 where Z is a sidechain of Formula ZH in which D⁴ is O or O--CH₂ are preferably prepared as described below in Reaction Scheme XXII. ##STR50## Preparation of Formula 807

As illustrated in Reaction Scheme XXII, Step 1, an aldehyde of Formula 302 (where Z⁵ is methyl) undergoes an aldol reaction with the bromo-alkyl oxazolidinone of Formula 806 (where q is 1 or 2), which can be prepared by analogy with the reactions described in J. Amer. Chem. Soc., 103, 2127, 1981, to give the acyloxazolidinone of Formula 807.

An oxazolidinone of Formula 806 is reacted with an equimolar amount of a base (such as lithium diisopropylamide or preferably di-n-butylboryl trifluoromethane sulphonate/triethylamine), and then with an aldehyde of Formula 302. The reaction takes place at -78° C. to 0° C. (preferably -40° C.) for 1 to 12 hours (preferably 3 hours) to afford the corresponding acyloxazolidinone of Formula 807.

Preparation of Formula 808

As illustrated in Reaction Scheme XXII, Step 2, an acyloxazolidinone of Formula 807 is hydrolyzed to the carboxylic acid of Formula 808.

An acyloxazolidinone of Formula 807 is reacted with 1-5 (preferably 3) molar equivalents of lithium hydroxide in 3:1 tetrahydrofuran containing 5-20 (preferably 12) molar equivalents of hydrogen peroxide. The reaction takes place at -10° to 25° C. (preferably 0° ) for 5 to 60 minutes (preferably 30 minutes) to give the corresponding carboxylic acid of Formula 808.

Preparation of Formula 809

As illustrated in Reaction Scheme XXII, Step 3, a carboxylic acid of Formula 808 is deprotected to give the corresponding phenol of Formula 809, using the method described with respect to Reaction Scheme X, Step 1.

Preparation of Formula 810

A phenol of Formula 809 is esterified to give the corresponding ester of Formula 810.

A phenol of Formula 809 is treated with methanol in the presence of 0.05 to 0.2 (preferably 0.1) molar equivalents of an acid catalyst (preferably p-toluenesulphonic acid). The reaction takes place at 0° to 50° C. (preferably 25° C.) for 1 to 24 hours (preferably 12 hours) to give the corresponding methyl ester of Formula 810.

Preparation of Formula 1H

A methyl ester of Formula 810 undergoes an intramolecular cyclization reaction to give the corresponding cyclized ester of Formula 1H.

A methyl ester of Formula 810 is treated with 1.9 to 2.5 (preferably 2.0) molar equivalents of a strong base (such as lithium diisopropylamide or preferably sodium hydride) in tetrahydrofuran (or preferably dimethylformamide). The reaction takes place at -10° to 25° C. (preferably 0° ) for 1-12 hours (preferably 2 hours) to give the corresponding cyclized ester of Formula 1H, which may be hydrolyzed to give the corresponding acid of Formula 1H, using the method described with respect to Reaction Scheme X, Step 2.

PREPARATION OF ESTERS OF FORMULA 1

The esters of Formula 1 (compounds where G is not OH) can be prepared as described in U.S. Pat. Nos. 4,727,069 and 4,753,935, incorporated herein by reference, by deprotection of a precursor (e.g., as described with reference to Reaction Scheme X, Steps 1) or as described below by attachment of a leaving group and its replacement by the desired ester.

PREPARATION OF INTERMEDIATES OF FORMULA A

The preparation of an intermediate of Formula A is shown in Reaction Scheme XXIII below. ##STR51## where R^(b) is a protecting group and Z^(a) is a sidechain of Formula Z as defined in the Summary of the Invention in which G is lower alkoxy. ##STR52## where Z^(b) is a sidechain of Formula Z as defined in the Summary of the Invention in which G is hydroxy. ##STR53## Preparation of Formula B

As illustrated in Reaction Scheme XXIII, Step 1, a lower alkyl ester of Formula 1, prepared as described above, is protected at the phenolic hydroxyl with an arylsulfonyl or alkylsulfonyl group.

A compound of Formula 1 is reacted with 1.0 to 1.1 (preferably 1.05) molar equivalents of an arylsulfonyl or alkylsulfonyl halide (preferably p-toluenesulfonyl chloride) in pyridine. The reaction takes place at -10° C. to 30° C. (preferably room temperature) for 1 to 24 hours (preferably 12 hours). The protected corresponding compound of Formula B is isolated by conventional means (such as evaporation).

Preparation of Formula C

As illustrated in Reaction Scheme XXIII, Step 2, a protected lower alkyl ester of Formula B is demethylated in a cleavage reaction with 5 moles of anhydrous lithium iodide in a pyridine solvent (preferably collidine). The reaction takes place at 50° to 75° C. (preferably 60° C.) for 10 hours to 8 days (preferably 4 days). The corresponding protected 6-hydroxy acid of Formula C is isolated by conventional means (such as evaporation).

Preparation of Formula D

As illustrated in Reaction Scheme XXIII, Step 3, a protected 6-hydroxy acid of Formula C is esterified in an acid-catalyzed esterification. The reaction takes place in a lower alkanol solvent (corresponding to the desired lower alkyl ester, such as methanol) with an acid (such as p-toluenesulfonic acid) at room temperature for 12 to 24 hours (preferably 18 hours). The corresponding protected 6-hydroxy lower alkyl ester of Formula D is isolated and purified by conventional means (such as chromatography).

Preparation of Formula E

As illustrated in Reaction Scheme XXIII, Step 4, a protected 6-hydroxy lower alkyl ester of Formula D is converted to the corresponding 6-triflate. The reaction takes place with the addition of 1.05 to 1.3 (preferably 1.2) molar equivalents of trifluoromethanesulfonic anhydride in a solvent (such as methylene chloride and/or pyridine) at -10° C. to 10° C. (preferably 0° C.) for 15 minutes to 10 hours (preferably 30 minutes). The corresponding protected 6-triflate of Formula E is isolated by conventional means (such as evaporation).

Preparation of Trialkylstannanes of Formula 5a

The trialkyl stannanes of Formula 5a are made by reaction of an organolithium or organomagnesium (Grignard) reagent with a trialkyl (preferably tributyl) tin chloride. The organolithium or organomagnesium reagents are either commercially available or are made conventionally, for example by halogen-metal exchange.

Compounds in which R⁷ contains a terminal triple bond can be reacted directly with butyllithiums to afford the organolithium compound.

The butyl lithium reaction takes place at -100° C. to 0° C. (preferably at -78° C.) for 1 to 8 hours (preferably 2 hours) to give the corresponding lithium derivative.

The halide starting material is reacted with magnesium metal in an ethereal solvent (preferably THF) under standard Grignard reaction conditions to give the magnesium halide derivative.

The lithium or magnesium halide derivative is reacted with a trialkylchlorostannane (preferably tributylchlorostannane) in an ethereal solvent (preferably THF). The reaction takes place at -78° C. to 0° C. for 1 to 4 hours (preferably 2 hours) to give the corresponding trialkylstannane of Formula 5a, which is isolated and used in Reaction Scheme A, Step 5 without further purification.

Tetramethyl, vinyltributyltin and phenyltributyl are all commercially available, e.g., from Aldrich.

Preparation of Formula F

As illustrated in Reaction Scheme XXIII, Step 5, a protected 6-triflate of Formula E is converted to the corresponding compound of Formula F where R⁷ is lower alkyl, cycloalkyl, vinyl, fluorovinyl, difluorovinyl, trifluorovinyl, alkenyl, --C.tbd.C--R¹¹, allenyl or CH₂ --O--(4-methoxybenzyl) by reaction with a trialkylstannane of Formula 5a in the presence of 6 moles of lithium chloride and a palladium catalyst [such as tris(dibenzylidineacetone)dipalladium (O) chloroform adduct, or preferably tetrakis-(triphenylphosphine)palladium]. The reaction takes place in a polar aprotic solvent (preferably N-methylpyrrolidinone) at 50° C. to 100° C. (preferably 80° C.) for 3 to 10 hours (preferably 6 hours). The 6-substituted protected lower alkyl ester of Formula F is isolated and purified by conventional methods.

The compounds of Formula F where R⁷ is lower alkyl of two or more carbon atoms can be made by hydrogenation of the corresponding alkenyl compounds of Formula F, e.g., as described below in Example 6.

Preparation of Formula A

As illustrated in Reaction Scheme XXIII, Step 6, a 6-substituted protected lower alkyl ester of Formula F is deprotected and converted to the corresponding acid by base hydrolysis. The compound of formula F is reacted with 5 moles of a strong base (preferably lithium hydroxide) in an aqueous/lower alkanol solvent (such as methanol:water). The reaction takes place at 50° to 70° C. (preferably 60° C.) for 10 to 24 hours (preferably 16 hours) followed by acidification. The 6-substituted acid of Formula A where Z^(b) is a sidechain of Formula Z as defined in the Summary of the Invention in which G is hydroxy is is isolated and purified by conventional means. This 6-substituted acid can be converted to a compound of Formula A where Z^(a) is a sidechain of Formula Z as defined in the Summary of the Invention in which G is lower alkoxy, by conventional means, for example as shown in Step 3 above.

Preparation of Formula A where R⁷ is CH₂ OH and CHO

The compounds of Formula A where R⁷ is CH₂ OH and CHO (respectively designated Formulae A-2 and A-3) are prepared as described with reference to Reaction Scheme XXIV. ##STR54## Preparation of Formula A-2

As illustrated in Reaction Scheme XXIV, Step 1, a 6-(4-methoxybenzyloxymethyl) substituted compound of Formula A (shown as Formula A-1) is debenzylated by reaction with 1 mole of a Lewis acid (such as boron tribromide or preferably boron trifluoride etherate), or with 20 moles of trifluoroacetic acid. The reaction takes place in dichloromethane at -10° C. to 5° C. (preferably 0° C.) for 30 minutes to 2 hours (preferably 1 hour). Alternatively, when using trifluoroacetic acid, the reaction takes place at room temperature. The corresponding 6-hydroxymethyl compound of Formula A-2 is isolated and purified by conventional means.

Preparation of Formula A-3

As illustrated in Reaction Scheme XXIV, Step 2, a 6-hydroxymethyl compound of Formula A-2 is oxidized (using manganese dioxide or preferably one mole of pyridine chlorochromate). The reaction takes place in methylene chloride at -10° C. to 5° C. (preferably 0° C.) for 8 to 24 hours (preferably 12 hours). The corresponding 6-formyl compound of Formula A-3 is isolated and purified by conventional means.

Alternative Preparation of Formula A where R⁷ is Lower Alkyl

A compound of Formula A where R⁷ is vinyl or alkenyl in converted to the corresponding lower alkyl compound by catalytic reduction in the presence of 0.01 to 0.10 (preferably 0.02) moles of tris(triphenylphosphine)rhodium chloride. The reaction takes place in an inert organic solvent (preferably 1:1 ethanol:benzene) at 20° C. to 30° C. (preferably 25° C.) for 1 to 12 hours (preferably 2 hours). The corresponding compound of Formula A where R⁷ is lower alkyl (other than methyl) is isolated and purified by conventional means.

Preparation of Intermediates of Formula 6

The preparation of a compound of Formula 6 is shown in Reaction Scheme XXV below. ##STR55## Preparation of Compounds of Formula 2

As illustrated in Reaction Scheme X/V, Step 1, a phenol of Formula A is converted to the trifluoromethylsulfonyl compound of Formula 2.

A compound of Formula A is reacted in an inert organic solvent, preferably dichloromethane, with about 1 to 3 molar equivalents, preferably about 2 molar equivalents, of a base, preferably pyridine, and with a slight excess, preferably about 1.1 molar equivalents, of a sulfonic anhydride, (such as a halo lower alkyl sulfonic anhydride, halomethyl sulfonic anhydride, and halosulfonic anhydride, or preferably trifluoromethanesulfonic anhydride or fluorosulfonic anhydride) or a sulfonyl halide, (such as trifluoromethylsulfonyl bromide, preferably trifluoromethylsulfonyl chloride). The reaction is carried out in the temperature range from about -20° C. to 20° C., preferably at about 0° C., for about 15 to 45 minutes, preferably about 30 minutes. The trifluoromethylsulfonyl reaction product, a compound of Formula 2, is isolated and purified by conventional means.

Preparation of Compounds of Formula 3

As illustrated in Reaction Scheme XXV, Step 2, a trifluoromethylsulfonyl derivative of Formula 2 is converted to the cyano compound of Formula 3.

A compound of Formula 2 is reacted with about 1 to 3 molar equivalents, preferably about 1.85 molar equivalents, of potassium cyanide with a catalytic amount of a triarylphosphine palladium complex, preferably tetrakis(triphenylphosphine) palladium, in an organic solvent, preferably 1,4-dioxane. The reaction is carried out in the temperature range from about 70° C. to 130° C., preferably at about the reflux temperature of 1,4-dioxane, for about 10 to 30 hours, preferably about 18 hours. The cyano reaction product, a compound of Formula 3, is isolated and purified by conventional means, preferably by extraction by an organic solvent and column chromatography.

Preparation of Compounds of Formula 4

As illustrated in Reaction Scheme XXV, Step 3, the cyano compound of Formula 3 is hydrolyzed to the carboxy compound of Formula 4.

A compound of Formula 3 is hydrolyzed by reacting it with about 1 to 10 molar equivalents, preferably about 4 molar equivalents, of an inorganic base (e.g., sodium hydroxide, lithium hydroxide, or potassium hydroxide, preferably sodium hydroxide,) in a large excess of organic solvent, preferably in about 3:2 water:methanol solution. The reaction is carried out in the temperature range from about 40° C. to 130° C., preferably at about the reflux temperature of the 3:2 water/methanol solvent, for about 1 to 3 hours, preferably about 2 hours. The reaction solution is distilled, and an additional of about 1 to 1.6 molar equivalents, preferably about 1.3 molar equivalents, of an inorganic base (e.g., sodium hydroxide, lithium hydroxide, or potassium hydroxide, preferably sodium hydroxide,) is added and the reaction is continued in the temperature range from about 40° C. to 130° C., preferably at about the reflux temperature of the remaining solution, for about 1 to 3 days, preferably about 2 days. The reaction product, a compound of Formula 4, is isolated and purified by conventional means.

Alternatively, the compound of Formula 4 may be prepared by reacting a corresponding compound of Formula 2 with a catalytic amount of 1,1'-bis (diphenylphosphine)ferrocene palladium dichloride in a large excess of an alkanol (preferably methanol) in an organic solvent (preferably trimethyl formamide) with a slight excess, preferably 1.01 molar equivalents, of an organic base (preferably triethylamine), under a carbon monoxide atmosphere of increased pressure of about 400-1000 PSI, preferably at about 600 PSI. The reaction product, which is a diester of a compound of Formula 5, is then hydrolyzed by reacting it with about 1 to 10 molar equivalents, preferably about 4 molar equivalents, of an inorganic base, preferably aqueous lithium hydroxide, in a large excess of an organic solvent, preferably 4:1 methanol/water solution. The solution is heated to a temperature range from about 30° C. to 80° C., preferably from about 50° C. to 60° C., for about 1 to 10 hours, preferably for about 2 to 6 hours. The reaction product, a compound of Formula 4, is isolated and purified by conventional means.

Preparation of Compounds of Formula 5

As illustrated in Reaction Scheme XXV, Step 4, a carboxy derivative of Formula 4 is converted to the ester of Formula 5.

The compound of Formula 4 is reacted in a large excess of a compound of the formula GH, where G is lower alkoxy, preferably methanol, with catalytic amounts of an acid catalyst, preferably p-toluenesulfonic acid. The reaction is carried out in the temperature range from about 0° C. to 40° C., preferably at about 20° C., for about 4 hours to 3 days, preferably about 24 hours. The reaction product, a 4-carboxy derivative of Formula 5, is isolated and purified by conventional means.

Preparation of Compounds of Formula 6

As illustrated in Reaction Scheme XXV, Step 5, a 4-carboxy derivative of Formula 5 is converted to the 4-isocyanate derivative of Formula 6.

A compound of Formula 5 is reacted with about 1 to 3 molar equivalents, preferably about 2 molar equivalents, of an organic base, preferably triethylamine, in a large excess of an organic solvent, preferably dimethylformamide, and about 1 to 2 molar equivalents, preferably about 1.3 molar equivalents, of an alkyl or phenyl haloformate or of a dialkyl or diphenyl halophosphate, preferably diphenyl chlorophosphate, in the temperature range from about -20° C. to 20° C., preferably at about 0° C., allowing it to warm to the temperature range from about 0° C. to 40° C., preferably at about 20° C., allowing the reaction to proceed for about 0.5 to 2 hours, preferably about I hour. The reaction mixture is recooled to the temperature range from about -20° C. to 20° C., preferably at about 0° C., and a large excess of sodium azide is added and the reaction proceeds for about 10 to 30 hours, preferably about 18 hours. The isocyanato reaction product, a compound of Formula 6, is isolated and purified by conventional means.

Alternatively, a compound of Formula 5 is reacted with about 1 to 3 molar equivalents, preferably about 2 molar equivalents, of an organic base, preferably triethylamine, in a large excess of an organic solvent, preferably dimethylformamide, and with a slight excess, preferably 1.2 molar equivalents, of a diphenyl or dialkyl phosphoroazide, preferably diphenyl phosphoroazide, in the temperature range from about 0° C. to 40° C., preferably at about 20° C., for about 12 to 36 hours, preferably for about 24 hours. The isocyanato reaction product, a compound of Formula 6, is isolated and purified by conventional means.

PREPARATION OF COMPOUNDS OF FORMULA I

In the following Reaction Schemes, it should be noted that Z^(a) represents a sidechain of Formula Z as defined in the Summary of the Invention in which G is lower alkoxy, and Z^(b) represents a sidechain of Formula Z as defined in the Summary of the Invention in which G is hydroxy.

1. Preparation of Compounds of Formula I where R¹ and R² are both Hydrogen

Compounds of Formula I where R¹ and R² are both hydrogen are depicted as Formula IA: ##STR56##

The preparation of compounds of Formula IA is shown in Reaction Scheme XXVI below. ##STR57## Preparation of Formula IA where Z is Z^(b)

A compound of Formula 6 is hydrolyzed with about I to 20 molar equivalents, preferably 10 molar equivalents, of an inorganic base, preferably lithium hydroxide monohydrate, in an inert organic solvent, preferably 3:10 water:l,4-dioxane. The reaction is carried out in the temperature range from about 0° C. to 40° C., preferably at about 20° C., for about 1 to 3 hours, preferably about 2 hours. The reaction product, a 4-amino compound of Formula IA where Z is Z^(b), is isolated and purified by conventional means, preferably column chromatography.

Preparation of Formula IA where Z is Z^(a)

A compound of Formula IA where Z is Z^(b) is esterified with a lower alkanol of formula GH, where G is lower alkoxy, as described in the preparation of a compound of Formula D.

Preparation of Compounds of Formula I where R¹ is Hydrogen and R² is --C(O)NR⁴ R⁵

Compounds of Formula I where R¹ is hydrogen and R² is --C(O)NR⁴ R⁵ are depicted as Formula IB: ##STR58##

The preparation of compounds of Formula IB is shown in Reaction Scheme XXVII below. ##STR59## Preparation of Formula IB where Z is Z^(a)

A compound of Formula 6 is reacted with a large excess of an amine compound of the formula HNR⁴ R⁵, where R⁴ and R⁵ are as defined in the Summary of Invention, for example, methylamine, dimethylamine, methylphenylamine, ammonia, and the like, in an inert organic solvent, preferably tetrahydrofuran. The reaction is carried out in the temperature range from about 0° C. to 40° C., preferably at about 20° C., for about 30 minutes to 2 hours, preferably about 1 hour. The reaction product, a 4-(optionally substituted ureido) ester of Formula IB where Z is Z^(a), is isolated and purified by conventional means.

Preparation of Formula IB where Z is Z^(b)

An ester of Formula IB is hydrolyzed by reacting with about 1 to 10 molar equivalents, preferably about 4 molar equivalents of an inorganic base, preferably aqueous lithium hydroxide, in a large excess of an organic solvent, preferably 4:1 methanol/water. The solution is heated to a temperature range from about 30° C. to 80° C., preferably from about 50° C. to 60° C., for about 1 to 10 hours, preferably for about 2 to 6 hours. The reaction product, a 4-(optionally substituted ureido) acid compound of Formula IB, is isolated and purified by conventional means.

Preparation of Compounds of Formula I where R¹ is Hydrogen and R² is --C(O)R³

Compounds of Formula I where R¹ is hydrogen and R² is --C(O)R³ are depicted as Formula IC: ##STR60##

The preparation of compounds of Formula IC is shown in Reaction Scheme XXVIII below. ##STR61## Preparation of Compounds of Formula IC where Z is Z^(a)

A compound of Formula IA is reacted in a large excess of an inert organic solvent, preferably dichloromethane, with about 1 to 6 molar equivalents, preferably about 2.5 molar equivalents, of an anhydride compound of the formula (R³ C(O))₂ O or of a acyl chloride of the formula R³ C(O)Cl, where R³ is as defined in the Summary of the Invention. The reaction is carried out in the temperature range from about 0° C. to 40° C., preferably at about 20° C., for about 30 minutes to 2 hours, preferably about 1 hour. The reaction product, an amido ester of Formula IC, is isolated and purified by conventional means, preferably by recrystallization.

Preparation of Formula IC where Z is Z^(b)

A compound of Formula IC as an ester is hydrolyzed as described in the preparation of a compound of Formula IB to give a 4-amido compound of Formula IC as a carboxylic acid.

Preparation of Compounds of Formula I where R¹ is Lower Alkyl and R² is --C(O)R³

Compounds of Formula I where R¹ is lower alkyl and R² is --C(O)R³ are depicted as Formula ID: ##STR62##

The preparation of compounds of Formula ID is shown in Reaction Scheme XXIX below. ##STR63## Preparation of Formula ID wherein R¹ is Lower Alkyl and Z is Z^(a)

A compound of Formula IC is reacted with about 1 to 10 molar equivalents, preferably about 4.5 molar equivalents, of a weak base, preferably potassium carbonate, and with about 1 to 10 molar equivalents, preferably about 4 molar equivalents, of a lower alkyl bromide or iodide, preferably an iodide, in an inert organic solvent, preferably dimethylformamide. The reaction is carried out in the temperature range from about 0° C. to 40° C., preferably at about 20° C., for about 12 to 48 hours, preferably about 24 hours. The organic layer is purified and then concentrated to an oil, to give an amide ester of Formula ID where R¹ is lower alkyl and G is lower alkoxy.

Preparation of Formula ID wherein R¹ is Lower Alkyl and Z is Z^(b)

An ester of Formula ID where R¹ is lower alkyl is hydrolyzed as described in the preparation of a compound of Formula IB to give a carboxylic acid of Formula ID where R¹ is lower alkyl.

Preparation of Compounds of Formula I where R¹ is Lower Alkyl and R² is Hydrogen

Compounds of Formula I where R¹ is lower alkyl and R² is hydrogen are depicted as Formula IE: ##STR64##

The preparation of compounds of Formula IE is shown in Reaction Scheme XXX below. ##STR65## Preparation of Formula IE where R¹ is Lower Alkyl and Z is Z^(b)

An amido ester of Formula ID is hydrolyzed by reacting with about 1 to 10 molar equivalents, preferably about 4 molar equivalents of an inorganic base (for example sodium hydroxide, preferably lithium hydroxide), in a large excess of an organic solvent, preferably 4:1 methanol/water. The solution is heated to a temperature range from about 50° C. to 100° C., preferably from about 60° C. to 80° C., for about 4 to 24 hours, preferably for about 12 hours. The reaction product, a 4-alkylamino acid compound of Formula IE, is isolated and purified by conventional means.

Preparation of Compounds of Formula I where G is Lower Alkoxy, Lower Thioalkoxy, or --(CH₂)_(m) --N═Y

The compounds of Formula I where G is lower alkoxy, lower thioalkoxy, or --O--(CH₂)_(m) --N═Y (i.e., the ester derivatives) may be prepared from the corresponding compounds of Formula I where G is hydroxy, including compounds of Formulae IA, IB, IC, ID, and IE, by conventional means, for example as described in the preparation of a compound of Formula D.

Preferred Preparation of Esters of Formula I where G is --O--(CH₂)_(m) --N═Y

In a preferred procedure, a compound of Formula I where G is hydroxy is esterified with an heterocyclic aminoalkyl alcohol of the formula GH, where G is --O--(CH₂)_(m) --N═Y, in which m and Y are as defined in the Summary of the Invention, by the direct esterification procedure described in the pending application entitled "Direct Esterification of Mycophenolic Acid", Ser. No. 07/911635, filed Jul. 10, 1992.

In the direct esterification route, an acid compound of Formula I where G is hydroxy is esterified slowly in a refluxing inert organic solvent capable of azeotropic removal of water (such as toluene, xylene, or a mixture thereof) using only a slight excess (between 1.01 to 1.20 molar equivalents, and preferably, 1.05 to 1.06 molar equivalents) of an heterocyclic aminoalkyl alcohol of the formula HO(CH₂)_(m) --N═Y. Water generated by the reaction is removed azeotropically.

For example, with toluene as the solvent: 1) the reaction takes place with (a) a reaction time of 20 to 120 hours, preferably 50 to 100 hours and most preferably 100 hours and (b) an initial pot temperature range of 114° to 120° C. increasing to a final pot temperature range of 118° to 130° C., preferably an initial pot temperature range of 115° to 118° C. increasing to a final pot temperature range of 118° to 125° C., each depending on solute concentration and atmospheric pressure, and most preferably an initial pot temperature of 116° C. increasing to a final pot temperature of 121° C. with a ratio of the acid compound of Formula I (where G is hydroxy) to toluene of 1 gm:2 ml at one atmosphere of pressure. The reaction product, a compound of Formula I where G is --O--(CH₂)_(m) --N═Y, is isolated and purified by conventional means.

Salts of Compounds of Formula I

Some of the compounds of Formula I may be converted to corresponding base addition salts by virtue of the presence of a carboxylic acid group. The conversion is accomplished by treatment with a stoichiometric amount of an appropriate base, such as potassium carbonate, sodium bicarbonate, ammonia, ethylenediamine, monoethanolamine, diethanolamine, triethanolamine and the like. Typically, the free acid is dissolved in a polar organic solvent such as ethanol, methanol or ethyl acetate, and the base added in water, ethanol, methanol or isopropanol. The temperature is maintained at about 0° C. to 50° C. The resulting salt precipitates spontaneously or may be brought out of solution with a less polar solvent.

The base addition salts of the compounds of Formula I may be decomposed to the corresponding free acids by treating with at least a stoichiometric amount of a suitable acid, such as hydrochloric acid or sulfuric acid, typically in the presence of aqueous solvent, and at a temperature of between about 0° C. and 50° C. The free acid form is isolated by conventional means, such as extraction with an organic solvent.

By virtue of the presence of an amine group in the 4-position, some of the compounds of Formula I may be converted to the acid addition salts by the substitution of an organic or inorganic acid for the base in the above procedure. The acid salts can be decomposed to the corresponding free bases by similar treatment with an appropriate base.

Preferred Processes

In summary, compounds of Formula I are prepared according to the following last steps:

1. A process for preparing compounds of Formula I,

wherein:

R¹ is hydrogen or lower alkyl;

R² is hydrogen, lower alkyl, --C(O)R³, --C(O)NR⁴ R⁵, --CO₂ R⁶, or --SO₂ R³ ; in

which:

R³ is hydrogen, lower alkyl, halo lower alkyl or optionally substituted phenyl;

R⁴ is hydrogen, lower alkyl or optionally substituted phenyl;

R⁵ is hydrogen, lower alkyl or optionally substituted phenyl;

R⁶ is lower alkyl or optionally substituted phenyl;

R⁷ is lower alkyl, cycloalkyl, fluorovinyl, difluorovinyl, trifluorovinyl, lower alkenyl, --C.tbd.C--, allyl, CHO, or CH₂ OR⁹ ; in which:

R⁸ is hydrogen or lower alkyl, and

R⁹ is hydrogen or 4-methoxybenzyl; and

Z is as defined in the Summary of the Invention, in which G is hydroxy:

comprises:

reacting a compound of the formula: ##STR66## where Z is as defined in the Summary of the Invention, in which G is lower alkoxy, lower thioalkyl, NG¹ G², O--(CH₂)_(n) --NG¹ G² or --O--(CH₂)_(n) --N═G³, in which n, G¹, G², and G³ are as defined in the Summary of the Invention; with an inorganic base.

2. Alternatively, a process for preparing compounds of Formula I,

wherein:

R¹, R², and R⁷ are as defined above, and G is lower alkoxy, lower thioalkyl NG¹ G², O--(CH₂)_(n) --NG¹ G², or O--(CH₂)_(n) --N═G³, in which n, G¹, G², and G³ are as defined in the Summary of the Invention;

comprises:

reacting a compound of the formula: ##STR67## where Z is as defined in the Summary of the Invention, in which G is hydroxy, with a compound of the formula GH, where G is as defined above, except that G cannot be hydroxy.

3. Alternatively, a process for preparing compounds of Formula I,

wherein:

R¹ is hydrogen;

R² is --C(O)NR⁴ R⁵, where R⁴ and R⁵ are independently hydrogen, lower alkyl or optionally substituted phenyl;

R⁷ is as defined above, and Z is as defined in the Summary of the Invention, in which G is lower alkoxy:

comprises:

reacting a compound of the formula: ##STR68## where Z is as defined in the Summary of the Invention, in which G is lower alkoxy:

with a compound of the formula HNR⁴ R⁵, where R⁴ and R⁵ are as defined above.

4. Alternatively, a process for preparing compounds of Formula I,

wherein:

R¹ is hydrogen;

R² is --C(O)R³, where R³ is lower alkyl, halo lower alkyl or optionally substituted phenyl;

R⁷ is as defined above, and Z is as defined in the Summary of the Invention, in which G is lower alkyl, optionally substituted phenyl, or --(CH₂)_(m) --N═Y,;

comprises:

reacting a compound of the formula: ##STR69## where R¹, R², R⁷, and Z are as defined above; with a compound of the formula (R³ C(O))₂ O or R³ C(O)Cl.

5. Alternatively, a process for preparing compounds of Formula I,

wherein:

R¹ is lower alkyl;

R² is --C(O)R³, where R³ is lower alkyl, halo lower alkyl or optionally substituted phenyl;

R⁷ is as defined above, and Z is as defined in the Summary of the Invention, in which G is lower alkoxy:

comprises:

reacting a compound of the formula: ##STR70## where Z is as defined in the Summary of the Invention, in which G is lower alkoxy:

with a compound of the formula R¹ X, where R¹ is lower alkyl and X is iodine or bromine.

Preferred Compounds

Among the family of compounds of the present invention, one preferred category includes the compounds where Z is a sidechain of Formula ZA, ZB, ZE, and ZH, especially where R⁷ is methyl, ethyl, vinyl, or cyclopropyl. Within this category a preferred group includes the compounds where R¹ is hydrogen, and R² is hydrogen or trifluoroacetyl, especially where G is hydroxy or morpholinoethoxy. Within this group one preferred subgroup includes the compounds where Z is ZA and R⁷ is ethyl, especially where Z¹ is methyl, Z² is hydrogen or methyl, and Z³ and Z⁴ are hydrogen.

Another preferred subgroup includes the compounds where Z is ZB, and R⁷ is ethyl, especially where D1--D² is --(CH₂)₃ -- and Z⁵ and Z⁸ are hydrogen, more especially where R² is hydrogen.

A third preferred subgroup includes the compounds where Z is ZE and R⁷ is ethyl, especially where Z⁵ and Z⁷ are hydrogen and Z⁶ is hydrogen or lower alkyl.

A fourth preferred subgroup includes the compounds where Z is ZH and R⁷ is ethyl, especially where Z¹ is lower alkyl and D⁴ is --CH₂ --, --CH₂ CH₂ --, or --O--CH₂ --.

At present, the most preferred compounds are:

(E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5yl)-4-methyl-4-hexenoic acid;

(E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoic acid; and

(E)-2-{2-[2-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-ethylidene]-cyclopent-1-yl}acetic acid.

Utility, Testing and Administration

General Utility

The compounds of the present invention, the pharmaceutically acceptable salts thereof and pharmaceutical compositions therewith (collectively the "compounds" for purposes of the following description) are useful as immunosuppressive agents, anti-inflammatory agents, anti-tumor agents, anti-proliferative agents, anti-viral agents and anti-psoriatic agents in mammals, whether domestic (cattle, pigs, sheep, goats, horses), pets (cats, dogs), or preferably humans. The compounds are inhibitors of inosine monophosphate dehydrogenase (IMPDH) and thus inhibit de novo purine synthesis; they have anti-proliferative effects (e.g., against smooth muscle cells and both B and T lymphocytes) and inhibit antibody formation and the glycosylation of cell adhesion molecules in lymphocytes and endothelial cells.

As immunosuppressive agents, the compounds are useful in treating auto-immune related disorders, for example: Type I Diabetes Mellitus; Inflammatory Bowel Disease (e.g., Crohn's Disease and Ulcerative Coliris); Systemic Lupus Erythematosus; Chronic Active Hepatitis; Multiple Sclerosis; Grave's Disease; Hashimoto's Thyroidiris; Behcet's Syndrome; Myasthenia Gravis; Sjogren's Syndrome; Pernicious Anemia; Idiopathic Adrenal Insufficiency; and Polyglandular Autoimmune Syndromes Type I and II.

The compounds are also useful as therapeutic immunosuppressive agents in the treatment of Asthma, Immunohemolytic Anemia, Glomerulonephritis, and Hepatitis. Preventative uses of the compounds as immunosuppressive agents include the treatment of allograft rejection, for example, in cardiac, lung, pancreatic, renal, liver, skin and corneal allografts, and prevention of Graft vs. Host Disease.

The compounds are useful for inhibiting proliferative responses to vascular injury, for example, stenosis following an insult to a blood vessel wall in post-angioplasty restenosis, and post-cardiac by-pass surgery restenosis.

The compounds are useful as anti-inflammatory agents, for example, in treating Rheumatoid Arthritis, Juvenile Rheumatoid Arthritis and Uveitis.

As anti-tumor agents, the compounds are useful in treating solid tumors and malignancies of lymphoreticular origin. For example, the compounds' utility for treatment of solid tumors includes: cancers of the head and neck, including squamous cell carcinoma; lung cancer, including small cell and non-small cell lung carcinoma; mediastinal tumors; esophageal cancer, including squamous cell carcinoma and adenocarcinoma; pancreatic cancer; cancer of the hepatobiliary system, including hepatocellular carcinoma, cholangiocarcinoma, gall bladder carcinoma and biliary tract carcinoma; small intestinal carcinoma, including adenocarcinoma, sarcoma, lymphoma and carcinoids; colorectal cancer, including colon carcinoma and rectal carcinoma; metastatic carcinoma; cancers of the genitourinary system, including ovarian cancer, uterine sarcoma, and renal cell, ureteral, bladder, prostate, urethral, penile, testicular, vulvar, vaginal, cervical, endometrial, and fallopian tube carcinoma; breast cancer; endocrine system cancer; soft tissue sarcomas; malignant mesotheliomas; skin cancer, including squamous cell carcinoma, basal cell carcinoma and melanoma; cancer of the central nervous system; malignant bone tumors; and plasma cell neoplasms.

As anti-tumor agents for the treatment of malignancies of lymphoreticular origin, the compounds are useful in treating, for example: Lymphomas and Leukemias, including B, T and promonocyte cell line malignancies, Mycoses Fungoides, Non-Hodgkins Lymphoma, Malignancies of Burkitt Lymphoma Cells and other EBV-transformed B-lymphocytes, Lymphomas resulting from Epstein-Barr viral infections in allograft recipients, Chronic Lymphocytic Leukemia, Acute Lymphocytic Leukemia and Hairy Cell Leukemia.

As anti-viral agents, the compounds are useful in treating, for example: retroviruses, including Human T-leukemia Viruses, Types I and II (HTLV-1 and HTLV-2), Human Immuno Deficiency Viruses, Types I and II (HIV-1, HIV-2) and, Human Nasopharyngeal Carcinoma Virus (NPCV) and in treating Herpes Viruses, including EBV infected B-lymphocytes, CMV infection, Herpes Virus Type 6, Herpes Simplex, Types 1 and 2, (HSV-1, HSV-2) and Herpes Zoster.

As anti-psoriatic agents, the compounds are useful in treating, for example, psoriasis and psoriatic arthritis. Testing

Activity testing is conducted as described in the following references, and by modifications thereof.

General anti-inflammatory, anti-viral, anti-tumor, anti-psoriatic and/or immunosuppressive activity is associated with the inhibition of Inosine 5'-Monophosphate Dehydrogenase ("IMPDH"). In vitro assays measuring the inhibition of IMPDH, for example, by determining the level of NADH formation according to the method of Anderson, J. H. and Sartorelli, A. C., J. Biol. Chem., 243:4762-4768 (1968) are predictive of such activity.

Initial animal screening tests to determine anti-inflammatory activity potential include the adjuvant arthritis assay, e.g., according to the method of Pearson, Proc. Soc. Exp. Biol. Med., 91:95-101 (1956). Also, in vitro tests, for example those using synovial explants from patients with rheumatoid arthritis, Dayer, et al., J. Exp. Med., 145:1399-1404 (1977), are useful in determining whether compounds exhibit anti-inflammatory activity.

Autoimmune activity is determined, for example, utilizing experimental allergic encephalomyelitis, by a modification of a procedure initially described by Grieg, et. al., J. Pharmacol. Exp. Ther., 173:85 (1970).

Human clinical trials for efficacy in the treatment of asthma are conducted, e.g., as described by Erzurum, Leff, Cochran, et al. "Lack of benefit of methotrexate in severe, steroid-dependent asthma. A double-blind, placebo controlled study." Ann. Int. Med., 114:353-360 (1991).

Activity to prevent the rejection of organ or tissue allografts in experimental animals is determined, for example, as described by Hao, et al., J. Immunol., 139:4022-4026 (1987). In addition, U.S. Pat. No. 4,707,443 and EP 226062, incorporated herein by reference, also describe assays for activity in prevention of allograft rejection by detection of IL-2R levels. Human clinical trials to establish efficacy in preventing rejection of solid organ transplants (such as renal) are conducted, e.g., as described by Lindholm, Albrechtsen, Tufveson, et al., "A randomized trial of cyclosporin and prednisolone versus cyclosporin, azathioprine and prednisolone in primary cadaveric renal transplantation," Transplantation, 54:624-631 (1992). Human clinical trials for graft vs. host disease are conducted, e.g., as described by Storb, Deeg, Whitehead, et al., "Methotrexate and cyclosporin compared with cyclosporin alone for prophylaxis of acute graft versus host disease after marrow transplantation for leukemia." New England J. Med., 314:729-735 (1986).

Immunosuppressive activity is determined by both in vivo and in vitro procedures. In vivo activity is determined, e.g., utilizing a modification of the Jerne hemolytic plaque assay, [Jerne, et al., "The agar plaque technique for recognizing antibody producing cells," Cell-boundAntibodies, Amos, B. and Kaprowski, H. editors (Wistar Institute Press, Philadelphia) 1963, p. 109]. In vitro activity is determined, e.g., by an adaptation of the procedure described by Greaves, et al., "Activation of human T and B lymphocytes by polyclonal mitogens," Nature, 248:698-701 (1974).

Anti-viral activity is determined, for example, by the procedure described by Smee, et al. ["Anti-Herpesvirus Activity of the Acyclic Nucleoside 9-(1,3-Dihydroxy-2-Propoxymethyl) Guanine," Antimicrobial Agents and Chemotherapy, 23(5):676-682 (1983)], or as described by planterose ["Antiviral and cytotoxic effects of mycophenolic acid," Journal of General Virology, 4:629 (1969)].

Anti-viral activity can likewise be determined by measurement of reverse transcriptase activity, for example, according to the method described by Chen et al., Biochem. Pharm., 36:4361 (1987).

Human clinical trials for anti-HIV efficacy (together with clinical treatment scenarios) are described and cited, for example, by Sande, et al., "Antiretroviral Therapy for Adult HIV-Infected Patients," JAMA, 270(21):2583-2589 (1993). A large scale clinical trial can be conducted, e.g., as described by Volberding, P. A., et al. "Zidovudine in asymptomatic human immunodeficiency virus infection: a controlled trial in persons with fewer than 500 CD4 positive cells per cubic millimeter," New England J. Med., 322(14):941-949 (1990). A smaller scale (Phase I) clinical trial can be conducted, e.g., as described by Browne, et al., "2',3'-Didehydro-3'-deoxythymidine (d4T) in Patients with AIDS or AIDS-Related Complex: A Phase I Trial," J. Infectious Diseases, 167:21-29 (1993).

Tests for systemic activity in psoriasis can be carried out, for example, as described by Spatz, et al., "Mycophenolic acid in psoriasis," British Journal of Dermatology, 98:429 (1978).

Tests for anti-tumor activity can be performed, for example, as described by Carter, et al. ["Mycophenolic acid: an anticancer compound with unusual properties," Nature, 223:848 (1969)].

In vitro activity for treating stenosis is demonstrated, for example, by inhibiting the proliferation of smooth muscle cells, as established by the following human arterial smooth muscle cell proliferation assay. Human smooth muscle cells are grown in culture. A test group is treated with the test compound added at selected concentrations in fresh media. Both groups receive 2 μCi tritiated thymidine (³ HTdR), a radioisotope label. After 24 hours, the cells are harvested and the amount of label incorporated into DNA is counted by scintillation; this is compared for the test and control groups, the amount being proportional to cell proliferation. Inhibition of smooth muscle proliferation is established when the test group has a lower radioisotope count than the control group. The concentrations of test compound required to inhibit proliferation by 50% (the IC₅₀), and to inhibit proliferation by more than 95% are determined.

In vivo activity for treating stenosis is demonstrated, for example, in rat and pig models for arterial stenosis. In the rat model, a test group is treated with the test compound, starting 6 days before and continuing for 14 days after injury to the left carotid artery; the test group is compared to a control group receiving vehicle without the test compound. Injury is achieved by a gentle perfusion of air through a 10 mm long section of the left artery. The right artery is left intact. Arterial cross-sections (10 μm) are taken from both the left and right arteries of each subject, and the area of the vessel wall (endothelium, intima, media) is measured, The amount of vascular proliferation is calculated by subtracting the mean area of the intact, right carotid artery from the mean area of the injured, left carotid artery. Reduction in vascular proliferation is established when the test group shows less proliferation than the control group.

Human clinical trials for restenosis after coronary angioplasty are conducted, e.g., as described by Serruys, Rutsch, Heyndrickx, et al., "prevention of restenosis after percutaneous transluminal coronary antioplasty with thromboxane A₂ -receptor blockade: a randomozed, double-blind, placebo-controlled trial." Circulation, 84:1568-80 (1991).

Administration

The compounds of Formula I are administered at a therapeutically effective dosage, e.g., a dosage sufficient to provide treatment for the disease states previously described. Administration of the compounds of the invention or the pharmaceutically acceptable salts thereof can be via any of the accepted modes of administration for agents that serve similar utilities. The compounds can be used both prophylactically (e.g., to prevent allograft rejection) and therapeutically.

While human dosage levels have yet to be optimized for the compounds of the invention, generally, a daily dose is from about 0.01 to 100.0 mg/kg of body weight, preferably about 0.1 to 64.3 mg/kg of body weight, and most preferably about 0.3 to 43.0 mg/kg of body weight. Thus, for administration to a 70 kg person, the dosage range would be about 0.7 mg to 7 g per day, preferably about 7.0 mg to 4.5 g per day, and most preferably about 21 mg to 3.0 g per day. The amount of active compound administered will, of course, be dependent on the subject and disease state being treated, the severity of the affliction, the manner and schedule of administration (e.g., oral administration one day prior to cancer chemotherapy and intravenous administration during cancer chemotherapy) and the judgment of the prescribing physician.

In employing the compounds of this invention for treatment of the above conditions, any pharmaceutically acceptable mode of administration can be used. The compounds of Formula I can be administered either alone or in combination with other pharmaceutically acceptable excipients, including solid, semi-solid, liquid or aerosol dosage forms, such as, for example, tablets, capsules, powders, liquids, injectables, suspensions, suppositories, aerosols or the like. The compounds of Formula I can also be administered in sustained or controlled release dosage forms, including depot injections, osmotic pumps, pills, transdermal (including electrotransport) patches, and the like, for the prolonged administration of the compound at a predetermined rate, preferably in unit dosage forms suitable for single administration of precise dosages. The compositions will typically include a conventional pharmaceutical carrier or excipient and a compound of Formula I or a pharmaceutically acceptable salt thereof. In addition, these compositions may include other medicinal agents, pharmaceutical agents, carriers, adjuvants, etc., such as multidrug resistance modifying agents, steroids, immunosuppressants such as cyclosporine A, azathioprene, rapamycin, FK-506, brequinar, leflunomide and vincrystine.

Generally, depending on the intended mode of administration, the pharmaceutically acceptable composition will contain about 0.1% to 90%, preferably about 0.5% to 50%, by weight of a compound or salt of Formula I, the remainder being suitable pharmaceutical excipients, carriers, etc.

One preferred manner of administration for the conditions detailed above is oral, using a convenient daily dosage regimen which can be adjusted according to the degree of affliction. For such oral administration, a pharmaceutically acceptable composition is formed by the incorporation of any of the normally employed excipients, such as, for example, mannitol, lactose, starch, povidone, magnesium stearate, sodium saccharine, talcum, cellulose, croscarmellose sodium, glucose, gelatin, sucrose, magnesium carbonate, and the like. Such compositions take the form of solutions, suspensions, tablets, dispersible tablets, pills, capsules, powders, sustained release formulations and the like.

Preferably the compositions will take the form of a pill or tablet and thus the composition will contain, along with the active ingredient, a diluent such as lactose, sucrose, dicalciumphosphate, or the like; a lubricant such as magnesium stearate or the like; a disintegrant such as croscarmellose sodium or the like; and a binder such as starch, gum acacia, polyvinylpyrrolidine, gelatin, cellulose and derivatives thereof, and the like.

Liquid pharmaceutically administrable compositions can, for example, be prepared by dissolving, dispersing, etc. an active compound as defined above and optional pharmaceutical adjuvants in a carrier, such as, for example, water, saline, aqueous dextrose, glycerol, glycols, ethanol, and the like, to thereby form a solution or suspension. If desired, the pharmaceutical composition to be administered may also contain minor amounts of nontoxic auxiliary substances such as wetting agents, suspending agents, emulsifying agents, or solubilizing agents, pH buffering agents and the like, for example, sodium acetate, sodium citrate, cyclodextrine derivatives, polyoxyethylene, sorbitan monolaurate or stearate, etc. Actual methods of preparing such dosage forms are known, or will be apparent, to those skilled in this art; for example, see Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa., 15th Edition, 1975. The composition or formulation to be administered will, in any event, contain a quantity of the active compound in an amount effective to alleviate the symptoms of the subject being treated.

Dosage forms or compositions containing active ingredient in the range of 0.005% to 95% with the balance made up from pharmaceutically acceptable carrier may be prepared.

For oral administration, a pharmaceutically acceptable composition is formed by the incorporation of any of the normally employed excipients, such as, for example pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, talcum, povidone, cellulose derivatives, croscarmellose sodium, glucose, sucrose, magnesium carbonate, sodium saccharin, talcum and the like. Such compositions take the form of solutions, suspensions, tablets, capsules, powders, sustained release formulations and the like. Such compositions may contain 0.01%-95% active ingredient, preferably 0.1-50%.

For a solid dosage form containing liquid, the solution or suspension, in for example propylene carbonate, vegetable oils or triglycerides, is preferably encapsulated in a gelatin capsule. Such ester solutions, and the preparation and encapsulation thereof, are disclosed in U.S. Pat. Nos. 4,328,245; 4,409,239; and 4,410,545. For a liquid dosage form, the solution, e.g. in a polyethylene glycol, may be diluted with a sufficient quantity of a pharmaceutically acceptable liquid carrier, e.g. water, to be easily measured for administration.

Alternatively, liquid or semi-solid oral formulations may be prepared by dissolving or dispersing the active compound or salt in vegetable oils, glycols, triglycerides, propylene glycol esters (e.g. propylene carbonate) and the like, and encapsulating these solutions or suspensions in hard or soft gelatin capsule shells.

Other useful formulations include those set forth in U.S. Pat. Nos. Re. 28,819 and 4,358,603.

Parenteral administration is generally characterized by injection, either subcutaneously, intramuscularly or intravenously. Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, solid forms suitable for solution or suspension in liquid prior to injection, or as emulsions. Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol or the like. In addition, if desired, the pharmaceutical compositions to be administered may also contain minor amounts of non-toxic auxiliary substances such as wetting or emulsifying agents, pH buffering agents, solubility enhancers, and the like, such as for example, sodium acetate, polyoxyethylene, sorbitan monolaurate, triethanolamine oleate, cyclodextrins, etc.

A more recently devised approach for parenteral administration employs the implantation of a slow-release or sustained-release system, such that a constant level of dosage is maintained. See, e.g., U.S. Pat. No. 3,710,795.

The percentage of active compound contained in such parenteral compositions is highly dependent on the specific nature thereof, as well as the activity of the compound and the needs of the subject. However, percentages of active ingredient of 0.01% to 10% in solution are employable, and will be higher if the composition is a solid which will be subsequently diluted to the above percentages. Preferably the composition will comprise 0.2-2% of the active agent in solution.

Formulations of the active compound or a salt may also be administered to the respiratory tract as an aerosol or solution for a nebulizer, or as a microfine powder for insufflation, alone or in combination with an inert carrier such as lactose. In such a case, the particles of the formulation have diameters of less than 50 microns, preferably less than 10 microns.

EXAMPLES

The following examples are given to enable those skilled in the art to more clearly understand and to practice the present invention. They should not be considered as limiting the scope of the invention, but merely as being illustrative and representative thereof.

Example 1 Preparation of Compounds of Formula B

1A. Formula B where Z^(a) is a Side Chain of Formula ZA in which G is Methoxy, and Z¹ is Methyl, Z², Z³, Z⁴ are Hydrogen, and R^(b) is Tosyl

p-Toluenesulfonyl chloride (30 g) was added to a solution of methyl (E) 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate (40 g) in pyridine (200 ml) at 0° C. After 6 hours the solution was poured on to ice and acidified to pH 3 with dilute hydrochloric acid. The solution was extracted with ethyl acetate and the extract was dried and evaporated to afford methyl (E) 6-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate.

1B. Formula B varying Z^(a)

By following the procedure of part A and substituting methyl (E) 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with:

methyl (E)-2-[2-[2-[1, 3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

ethyl (E)-3-[2-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(4-hydroxy-1,3-dihydro-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the compounds of Formula 1 where Z^(a) corresponds to the side chains identified in the following tables:

    ______________________________________                                          ##STR71##                                                                     Z.sup.1                                                                               Z.sup.2 Z.sup.3  Z.sup.4  Isomer                                        ______________________________________                                         Methyl H       H        Methyl                                                 Methyl Methyl  H        Ethyl                                                  Ethyl  H       H        H                                                      Ethyl  H       H        Methyl                                                 n-Propyl                                                                              H       H        Methyl                                                 CF.sub.3                                                                              H       H        Methyl                                                 CF.sub.3                                                                              H       H        H                                                      H      H       H        H                                                      H      H       H        Methyl                                                 Methyl Methyl  H        H                                                      H      Methyl  H        Methyl                                                 Methyl Methyl  H        Methyl   Diastereoisomer A                             Methyl Methyl  H        Methyl   Diastereoisomer B                             Methyl Methyl  H        Methyl   (+) Single Isomer                             Methyl H       H        Methyl   2 - (R) Isomer                                Methyl H       H        Methyl   2 - (S) Isomer                                Methyl H       H        Ethyl    2 - (S) Isomer                                Methyl H       H        Vinyl                                                  Methyl H       H        Allyl                                                  Methyl H       H        n-Propyl                                               Methyl H       H        iso-Propyl                                             Methyl H       H        Cyclopropyl                                            Methyl H       H        Cyclopropyl                                                                    methyl                                                 Methyl H       H        n-Butyl                                                Methyl H       H        sec-Butyl                                              Methyl H       H        2-Methoxy-                                                                     ethyl                                                  Methyl H       Phenyl   H                                                      Methyl H       Phenyl   Methyl                                                 Methyl H       Methoxy  H                                                      ______________________________________                                    

    ______________________________________                                          ##STR72##                                                                     Z.sup.1                                                                               Z.sup.2   Z.sup.3   Z.sup.4 Isomer                                      ______________________________________                                         Methyl H         Ethoxy    Ethyl                                               Methyl H         Methylthio                                                                               H                                                   Methyl H         Ethylthio Methyl                                              Methyl Methyl    H         H                                                   Methyl Ethyl     H         H                                                   Methyl Ethoxy    Methyl    H                                                   Methyl Ethoxy    H         H                                                   Methyl Ethoxy    H         Cl                                                  Methyl Ethoxy    H         Phenyl                                              Methyl Ethoxy    H         Ethyl                                               Ethyl  Methoxy   H         H                                                   CF.sub.3                                                                              n-Propoxy H         H                                                   Cl     Ethoxy    H         H                                                   Ethyl  H         t-Butyl   H       2 - (S) Isomer                              n-Propyl                                                                              H         Methyl    H       2 - (R) Isomer                              H      H         SO-Methyl H                                                   Methyl H         SO-Methyl H                                                   Methyl H         SO-Ethyl  H                                                   Methyl Methyl    SO-Methyl Methoxy                                             Methyl Methoxy   SO-Ethyl  Phenyl                                              CF.sub.3                                                                              H         SO-t-Butyl                                                                               H                                                   Cl     H         H         H                                                   Fl     H         H         H                                                   Cl     H         H         cyclopentyl                                         Methyl H         Cyclopropyl                                                   Methyl H         S-Methyl  H                                                   n-Propyl                                                                              H         S-Propyl  H                                                   Methyl Methyl    S-Ethyl   H                                                   ______________________________________                                    

    ______________________________________                                          ##STR73##                                                                     D.sup.1 -D.sup.2                                                                            Z.sup.5  Z.sup.8  Isomer                                          ______________________________________                                         (CH.sub.2).sub.2                                                                            H        H                                                        (CH.sub.2).sub.4                                                                            H        H                                                        (CH.sub.2).sub.5                                                                            H        H                                                        CH.sub.2 OCH.sub.2                                                                          H        H                                                        CH.sub.2 OCH.sub.2                                                                          Methyl   H        1 (S), 2 (S)                                                                   Isomer                                          CH.sub.2 OCH.sub.2                                                                          Methyl   H        1 (S), 2 (R)                                                                   Isomer                                          (CH.sub.2).sub.2 OCH.sub.2                                                                  H        H        (-) Isomer                                      (CH.sub.2).sub.2 OCH.sub.2                                                                  H        H        (+) Isomer                                      (CH.sub.2).sub.2 OCH.sub.2                                                                  H        H        (±) Isomer                                   CH.sub.2 SCH.sub.2                                                                          H        Methyl                                                   CH.sub.2 NHCH.sub.2                                                                         H        H                                                        (CH.sub.2).sub.2 S(O)CH.sub.2                                                               H        H                                                        (CH.sub.2).sub.2 OCH.sub.2                                                                  H        Methyl                                                   (CH.sub.2).sub.3 OCH.sub.2                                                                  H        H                                                        (CH.sub.2).sub.3                                                                            Methyl   H        Diastereomer A                                                        1 (S)                                                    (CH.sub.2).sub.3                                                                            Methyl   H        Diastereomer B                                                        1 (S)                                                    (CH.sub.2).sub.3                                                                            Ethyl    H        1 (S), 2 (R)                                                                   Isomer                                          (CH.sub.2).sub.3                                                                            Ethyl    H        1 (S), 2 (S)                                                                   Isomer                                          (CH.sub.2).sub.3                                                                            n-Propyl H                                                        (CH.sub.2).sub.4                                                                            Methyl   H        Diasteriomer A                                  (CH.sub.2).sub.4                                                                            Methyl   H        1 (S), 2 (R)                                                                   Isomer                                          (CH.sub.2).sub.4                                                                            Methyl   H        Diastereomer B                                  (CH.sub.2).sub.4                                                                            Methyl   H        1 (S), 2 (S)                                                                   Isomer                                          (CH.sub.2).sub.4                                                                            Ethyl    Methyl                                                   (CH.sub.2).sub.3                                                                            n-Hexyl  Methyl                                                   ______________________________________                                    

    ______________________________________                                          ##STR74##                                                                     Z.sup.5       Z.sup.6      Z.sup.7                                             ______________________________________                                         H             H            H                                                   H             3-Methyl     H                                                   H             6-Methyl     H                                                   H             5-t-Butyl    H                                                   H             5-Methyl     6-Methyl                                            H             5-Methoxy    H                                                   H             4-COOH       H                                                   H             4-Chloro     H                                                   H             5-Chloro     H                                                   H             5-Bromo      6-Bromo                                             H             5-Nitro      H                                                   H             6-Nitro      H                                                   Methyl        H            H                                                   Methyl        3-Methyl     H                                                   Methyl        6-Methyl     H                                                   Methyl        5-t-Butyl    H                                                   Methyl        5-Methyl     6-Methyl                                            Methyl        5-Methoxy    H                                                   Methyl        4-COOH       H                                                   Methyl        4-Chloro     H                                                   Methyl        5-Chloro     H                                                   Methyl        5-Bromo      6-Bromo                                             Methyl        6-Nitro      H                                                   n-Propyl      H            H                                                   n-Propyl      3-Methyl     H                                                   n-Propyl      6-Methyl     H                                                   n-Propyl      5-t-Butyl    H                                                   n-Propyl      5-Methyl     6-Methyl                                            n-Propyl      5-Methoxy    H                                                   n-Propyl      4-COOH       H                                                   ______________________________________                                    

    ______________________________________                                          ##STR75##                                                                            D.sup.4      Z.sup.1                                                    ______________________________________                                                CH.sub.2     Hydrogen                                                          OCH.sub.2    Methyl                                                            CH.sub.2     Ethyl                                                             CH.sub.2     n-Propyl                                                          (CH.sub.2).sub.2                                                                            H                                                                 (CH.sub.2).sub.2                                                                            Methyl                                                            (CH.sub.2).sub.2                                                                            Ethyl                                                             (CH.sub.2).sub.3                                                                            H                                                                 (CH.sub.2).sub.3                                                                            Methyl                                                            CH.sub.2     CF.sub.3                                                   ______________________________________                                    

there are obtained

methyl (E)-2-[2-[2-[1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxy-5-isobenzofuranylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

ethyl (E)-3-[2-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzo-furan-5-yl)cyclopent-1-en-1-yl]-p-propionate;

methyl (E)-2-[-3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other corresponding compounds of Formula B.

Example 2 Preparation of Compounds of Formula C

2A. Formula C where Z^(b) is a Side Chain of Formula ZA in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, and R^(b) is Tosyl

A solution of methyl (E) 6-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate (28 g) in 2,4,6-collidine (100 ml) was heated to 65° C. and lithium iodide (50 g) was added. After 3 days the solution was added to ethyl acetate and dilute hydrochloric acid. The organic layer was dried and evaporated to afford (E) 6-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

2B. Formula C Varying Z^(b)

By following the procedure of part A and substituting methyl (E) 6-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate with:

methyl (E)-2-[2-[2-[1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

ethyl (E)-3-[2-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-ptoluenesulfonyloxyisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other compounds of Formula B corresponding to those listed in the tables in Example 1B, there are obtained:

(E)-2-[2-[2-[1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetic acid;

3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyl-oxyisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetic acid;

(E)-3-[2-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluene-sulfonyloxyisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylic acid;

(E)-2-[3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoic acid;

4-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylic acid;

3-[3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionic acid;

(E)-2-[-3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylic acid;

and the other compounds of Formula C corresponding to those listed in the tables in Example 1B.

Example 3 Preparation of Compounds of Formula D

3A. Formula D where Z^(a) is a Side Chain of Formula ZA in which Z¹ is Methyl, Z², Z³, Z⁴ are Hydrogen, G is Methoxy, and R^(b) is Tosyl.

A solution of (E) 6-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoic acid (23 g) and p-toluenesulfonic acid (0.8 g) in methanol (150 ml) was stirred for 18 hours then added to water and ethyl acetate. The organc layer was dried and evaporated and the residue was chromatographed on silica gel, eluting with hexane:ethyl acetate: methanol 40:58:2, to afford methyl (E) 6-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate.

B. Formula D Varying Z^(a)

By following the procedure of part A and substituting (E) 6-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoic acid with:

(E)-2-[2-[2-[1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetic acid;

3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetic acid;

(E)-3-[2-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylic acid;

(E)-2-[3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoic acid;

4-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylic acid;

3-[3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionic acid;

(E)-2-[-3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylic acid;

and the other compounds of Formula C corresponding to those listed in the tables in Example 1B, there are obtained:

methyl (E)-2-[2-[2-[1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxy-5-isobenzofuranylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

methyl (E)-3-[2-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other compounds of Formula D corresponding to those listed in the tables in Example 1B.

Example 4 Preparation of Compounds of Formula E

4A. Formula E where Z^(a) is a Side Chain of Formula ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, G is Methoxy, and R^(b) is Tosyl

Trifluoromethanesulfonic anhydride (10.57 g) was added to a solution of methyl (E) 6-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate in methylene chloride (500 ml) and pyridine (5 ml) at 0° C. After 6 hours the reaction was added to excess aqueous sodium bicarbonate. The organic solution was dried and evaporated to afford methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate.

4B. Formula E Varying Z^(a)

By following the procedure of part A and substituting methyl (E) 6-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate with:

methyl (E)-2-[2-[2-[1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

methyl (E)-3-[2-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other compounds of Formula D corresponding to those listed in the tables in Example 1B, there are obtained:

methyl (E)-2-[2-[2-[1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxy-isobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyl-oxy-6-trifluoromethanesulfonyloxyisobenzo-furan-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

methyl (E)-3-[2-(1,3-dihydro-7-methyl-3-oxo-4-p-toluene-sulfonyloxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxy-isobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyl-oxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxy-isobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxy-isobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other compounds of Formula E corresponding to those listed in the tables in Example 1B.

Example 5 Preparation of Compounds of Formula F

5A. Formula F where Z^(a) is a Side Chain of Formula ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, G is Methoxy, R^(b) is Tosyl, and R⁷ is Vinyl

A mixture of lithium chloride (4.8 g), tris(dibenzylideneacetone)-dipalladium (0) chloroform adduct (0.65 g), triphenylarsine (1.6 g) and methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate (24.2 g) in N-methylpyrrolidinone (220 ml) was heated to 55° C. Vinyltributyltin (15 g) was added. After 3 hours the mixture was added to water (500 ml), potassium fluoride (16 g) and ethyl acetate. The organic solution was dried, filtered through celite and evaporated to afford methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate.

5B. Formula F Varying Z^(a)

By following the procedure of part A and substituting methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate with:

methyl (E)-2-[2-[2-[1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxy-isobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyl-oxy-6-trifluoromethanesulfonyloxyisobenzo-furan-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

methyl (E)-3-[2-(1,3-dihydro-7-methyl-3-oxo-4-p-toluene-sulfonyloxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxy-isobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyl-oxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxy-isobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxy-isobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other compounds of Formula E corresponding to those listed in the tables in Example 1B, there are obtained:

methyl (E)-2-[2-[2-[1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyl-oxy-6-vinylisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

methyl (E)-3-[2-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyl-oxy-6-vinylisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other compounds of Formula F corresponding to those listed in the tables in Example 1B.

C. Formula F Varying R⁷

By following the procedure of part A and substituting vinyltributyltin with:

methyltributyltin; cyclopropyltributyltin; fluorovinyltributyltin; trifluorovinyltributyltin; prop-2-enyltributyltin; ethynyltributyltin; pent-2-ynyltributyltin; allyltributyltin; and 4-methoxybenzyloxymethyltributyltin; there are obtained:

methyl (E) 6-(1,3-dihydro-6,7-dimethyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-cyclopropyl-1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-fluorovinyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethynyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(pent-2-ynyl)-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-allyl-1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(1,3-dihydro-6-methoxybenzyloxymethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate.

Example 6 Alternative Preparation of Compounds of Formula F

6A. Formula F where Z^(a) is a Side Chain of Formula ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, G is Methoxy, R^(b) is Tosyl, and R⁷ is Ethyl

A solution of methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate (17.7 g) and tris(triphenylphosphine) rhodium chloride (1.2 g) in benzene (180 ml) and ethanol (180 ml) was hydrogenated for 11 hours. The solvents were removed under vacuum and the residue was crystallized from ethyl acetate/tert butyl methyl ether to afford methyl (E) 6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate, mp 101.3°-102.8° C.

6B. Formula F where R⁷ is Ethyl, Varying Z^(a)

By following the procedure of part A and substituting methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate with:

methyl (E)-2-[2-[2-[1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyl-oxy-6-vinylisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

methyl (E)-3-[2-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other compounds of Formula F corresponding to those listed in the tables in Example 1B, there are obtained:

methyl (E)-2-[2-[2-[1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

methyl (E)-3-[2-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other compounds of Formula F where R⁷ is ethyl, corresponding to those listed in the tables in Example 1B.

Example 7 Preparation of Compounds of Formula A

7A. Formula A where Z^(b) is a Side Chain of Formula ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, and R⁷ is Vinyl

A solution of methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinyl isobenzofuran-5-yl)-4-methyl-4-hexenoate (0.37 g) and lithium hydroxide (0.4 g) in methanol (6 ml) and water (6 ml) was heated at 62° C. for 15 hours. The reaction was acidified with aqueous sodium hydrogen sulfate and extracted with ethyl acetate. The extract was dried and evaporated and the residue chromatographed on silica gel, eluting with ethyl acetate/hexane/acetic acid to give (E) 6-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoic acid, m.p. 148° 149° C. (tert-butylmethyl ether/hexane).

7B. Formula A Varying Z^(a)

By following the procedure of part A and substituting methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate with:

methyl (E)-2-[2-[2-[1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetate;

methyl 3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyl-oxy-6-vinylisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetate;

methyl (E)-3-[2-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylate;

methyl (E)-2-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoate;

methyl 4-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyl-oxy-6-vinylisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylate;

methyl 3-[3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)cyclopent-1-en-1-yl]-propionate;

methyl (E)-2-[-3-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-1-methylpropenyl]-cyclopentanecarboxylate;

and the other compounds of Formula F corresponding to those listed in the tables in Example 1B, there are obtained:

(E)-2-[2-[2-[1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl]ethylidene]cyclopent-1-yl]acetic acid;

3-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-vinylisobenzofuran-5-ylmethyl)-2-methylcyclopent-2-en-1-ylacetic acid;

(E)-3-[2-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl)ethylidene]cyclopentane-1-carboxylic acid;

(E)-2-[3-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl)-prop-1-en-1-yl]-3-methylbenzoic acid;

4-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-vinylisobenzofuran-5-ylmethyl)-3-methylcyclopent-3-ene-1-carboxylic acid;

3-[3-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-vinylisobenzo-furan-5-yl)cyclopent-1-en-1-yl]-propionic acid;

(E)-2-[-3-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-vinylisobenzofuran5-yl)-1-methylpropenyl]-cyclopentanecarboxylic acid;

and the other compounds of Formula A where R⁷ is vinyl, corresponding to those listed in the tables that follow:

    ______________________________________                                          ##STR76##                                                                     Z.sup.1 Z.sup.2 Z.sup.3                                                                               Z.sup.4  Isomer                                         ______________________________________                                         Methyl  H       H      Methyl                                                  Methyl  Methyl  H      Ethyl                                                   Ethyl   H       H      H                                                       Ethyl   H       H      Methyl                                                  n-Propyl                                                                               H       H      Methyl                                                  CF.sub.3                                                                               H       H      Methyl                                                  CF.sub.3                                                                               H       H      H                                                       H       H       H      H                                                       H       H       H      Methyl                                                  Methyl  Methyl  H      H                                                       H       Methyl  H      Methyl                                                  Methyl  Methyl  H      Methyl   Diastereoisomer A                              Methyl  Methyl  H      Methyl   Diastereoisomer B                              Methyl  Methyl  H      Methyl   (+) Single Isomer                              Methyl  H       H      Methyl   2 - (R) Isomer                                 Methyl  H       H      Methyl   2 - (S) Isomer                                 Methyl  H       H      Ethyl    2 - (S) Isomer                                 Methyl  H       H      Vinyl                                                   Methyl  H       H      Allyl                                                   Methyl  H       H      n-Propyl                                                Methyl  H       H      iso-Propyl                                              Methyl  H       H      Cyclopropyl                                             Methyl  H       H      Cyclopropyl                                                                    methyl                                                  Methyl  H       H      n-Butyl                                                 Methyl  H       H      sec-Butyl                                               Methyl  H       H      2-Methoxy-                                                                     ethyl                                                   Methyl  Ethyl   H      H                                                       ______________________________________                                    

    ______________________________________                                          ##STR77##                                                                     Z.sup.1 Z.sup.2   Z.sup.3   Z.sup.4                                                                               Isomer                                      ______________________________________                                         Methyl  H         Phenyl    H                                                  Methyl  H         Phenyl    Methyl                                             Methyl  H         Methoxy   H                                                  Methyl  H         Ethoxy    Ethyl                                              Methyl  H         Methylthio                                                                               H                                                  Methyl  H         Ethylthio Methyl                                             Methyl  Methyl    H         H                                                  H       Ethoxy    H         H                                                  Methyl  Ethoxy    Methyl    H                                                  Methyl  Ethoxy    H         H                                                  Methyl  Ethoxy    H         Cl                                                 Methyl  Ethoxy    H         Phenyl                                             Methyl  Ethoxy    H         Ethyl                                              Ethyl   Methoxy   H         H                                                  CF.sub.3                                                                               n-Propoxy H         H                                                  Cl      Ethoxy    H         H                                                  Ethyl   H         t-Butyl   H      2 - (S) Isomer                              n-Propyl                                                                               H         Methyl    H      2 - (R) Isomer                              H       H         SO-Methyl H                                                  Methyl  H         SO-Methyl H                                                  Methyl  H         SO-Ethyl  H                                                  Methyl  Methyl    SO-Methyl Methoxy                                            Methyl  Methoxy   SO-Ethyl  Phenyl                                             CF.sub.3                                                                               H         SO-t-Butyl                                                                               H                                                  Cl      H         H         H                                                  Fl      H         H         H                                                  Cl      H         H         cyclo-                                                                         pentyl                                             Methyl  H         Cyclopropyl                                                  Methyl  H         S-Methyl  H                                                  n-Propyl                                                                               H         S-Propyl  H                                                  ______________________________________                                    

    ______________________________________                                          ##STR78##                                                                     Z.sup.1 Z.sup.2  Z.sup.3   Z.sup.4  Isomer                                     ______________________________________                                         Methyl  Methyl   S-Ethyl   H                                                   ______________________________________                                    

    ______________________________________                                          ##STR79##                                                                     D.sup.1 -D.sup.2                                                                            Z.sup.5  Z.sup.8 Isomer                                           ______________________________________                                         (CH.sub.2).sub.2                                                                            H        H                                                        (CH.sub.2).sub.4                                                                            H        H                                                        (CH.sub.2).sub.5                                                                            H        H                                                        CH.sub.2 OCH.sub.2                                                                          H        H                                                        CH.sub.2 OCH.sub.2                                                                          Methyl   H       1 (S), 2 (S)                                                                   Isomer                                           CH.sub.2 OCH.sub.2                                                                          Methyl   H       1 (S), 2 (R)                                                                   Isomer                                           (CH.sub.2).sub.2 OCH.sub.2                                                                  H        H       (-) Isomer                                       (CH.sub.2).sub.2 OCH.sub.2                                                                  H        H       (+) Isomer                                       (CH.sub.2).sub.2 OCH.sub.2                                                                  H        H       (±) Isomer                                    CH.sub.2 SCH.sub.2                                                                          H        Methyl                                                   CH.sub.2 NHCH.sub.2                                                                         H        H                                                        (CH.sub.2).sub.2 S(O)CH.sub.2                                                               H        H                                                        (CH.sub.2).sub.2 OCH.sub.2                                                                  H        Methyl                                                   (CH.sub.2).sub.3 OCH.sub.2                                                                  H        H                                                        (CH.sub.2).sub.3                                                                            Methyl   H       Diastereomer A                                                         1 (S)                                                    (CH.sub.2).sub.3                                                                            Methyl   H       Diastereomer B                                                         1 (S)                                                    (CH.sub.2).sub.3                                                                            Ethyl    H       1 (S), 2 (R)                                                                   Isomer                                           (CH.sub.2).sub.3                                                                            Ethyl    H       1 (S), 2 (S)                                                                   Isomer                                           (CH.sub.2).sub.3                                                                            n-Propyl H                                                        ______________________________________                                    

    ______________________________________                                          ##STR80##                                                                     D.sup.1 -D.sup.2                                                                         Z.sup.5    Z.sup.8   Isomer                                          ______________________________________                                         (CH.sub.2).sub.4                                                                         Methyl     H         Diasteriomer A                                  (CH.sub.2).sub.4                                                                         Methyl     H         1 (S), 2 (R)                                                                   Isomer                                          (CH.sub.2).sub.4                                                                         Methyl     H         Diastereomer B                                  (CH.sub.2).sub.4                                                                         Methyl     H         1 (S), 2 (S)                                                                   Isomer                                          (CH.sub.2).sub.4                                                                         Ethyl      Methyl                                                    (CH.sub.2).sub.3                                                                         n-Hexyl    Methyl                                                    ______________________________________                                    

    ______________________________________                                          ##STR81##                                                                     Z.sup.5       Z.sup.6       Z.sup.7                                            ______________________________________                                         H             H             H                                                  H             3-Methyl      H                                                  H             6-Methyl      H                                                  H             5-t-Butyl     H                                                  H             5-Methyl      6-Methyl                                           H             5-Methoxy     H                                                  H             4-COOH        H                                                  H             4-Chloro      H                                                  H             5-Chloro      H                                                  H             5-Bromo       6-Bromo                                            H             5-Nitro       H                                                  H             6-Nitro       H                                                  Methyl        H             H                                                  Methyl        3-Methyl      H                                                  ______________________________________                                    

    ______________________________________                                          ##STR82##                                                                     Z.sup.5       Z.sup.6       Z.sup.7                                            ______________________________________                                         Methyl        6-Methyl      H                                                  Methyl        5-t-Butyl     H                                                  Methyl        5-Methyl      6-Methyl                                           Methyl        5-Methoxy     H                                                  Methyl        4-COOH        H                                                  Methyl        4-Chloro      H                                                  Methyl        5-Chloro      H                                                  Methyl        5-Bromo       6-Bromo                                            Methyl        6-Nitro       H                                                  n-Propyl      H             H                                                  n-Propyl      3-Methyl      H                                                  n-Propyl      6-Methyl      H                                                  n-Propyl      5-t-Butyl     H                                                  n-Propyl      5-Methyl      6-Methyl                                           n-Propyl      5-Methoxy     H                                                  n-Propyl      4-COOH        H                                                  n-Propyl      4-Chloro      H                                                  n-Propyl      5-Chloro      H                                                  n-Propyl      5-Bromo       6-Bromo                                            n-Propyl      6-Nitro       H                                                  ______________________________________                                    

    ______________________________________                                          ##STR83##                                                                            D.sup.4      Z.sup.1                                                    ______________________________________                                                CH.sub.2     Hydrogen                                                          OCH.sub.2    Methyl                                                            CH.sub.2     Ethyl                                                             CH.sub.2     n-Propyl                                                          (CH.sub.2).sub.2                                                                            H                                                                 (CH.sub.2).sub.2                                                                            Methyl                                                            (CH.sub.2).sub.2                                                                            Ethyl                                                             (CH.sub.2).sub.3                                                                            H                                                                 (CH.sub.2).sub.3                                                                            Methyl                                                            CH.sub.2     CF.sub.3                                                   ______________________________________                                    

7C. Formula A Varying R⁷

By following the procedure of part A and substituting methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate with:

methyl (E) 6-(1,3-dihydro-6,7-dimethyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-cyclopropyl-1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-fluorovinyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethynyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(pent-2-ynyl)-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-allyl-1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate. there are obtained:

(E) 6-(1,3-dihydro-4-hydroxy-6,7-dimethyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(6-cyclopropyl-1,3-dihydro-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(1,3-dihydro-6-fluorovinyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-(prop-2-enyl)isobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(1,3-dihydro-6-ethynyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(1,3-dihydro-4-hydroxy-7-methyl-3-oxo-6-(pent-2-ynyl)isobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(6-allyl-1,3-dihydro-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid; and

(E) 6-(1,3-dihydro-4-hydroxy-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

Example 9 Preparation of Compounds of Formula A where R⁷ is Hydromethyl and Formyl

9A. Preparation of Methyl (E) 6-(1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxo-4-p-toluenesulfonyloxyiso-benzofuran-5-yl)-4-methyl-4-hexenoate

A mixture of lithium chloride (1.6 g), tris (dibenzylideneacetone)dipalladium (0) chloroform adduct (0.22 g), triphenylarsine (0.53 g), methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxy-isobenzofuran-5-yl)-4-methyl-4-hexenoate (8.0 g) and N-methylpyrrolidinone (70 ml) is heated to 55° C.

p-Methoxybenzyloxymethyltributyltin (7.5 g) is added. After 3 hours the solution is added to water (200 ml), potassium fluoride (5 g) and ethyl acetate (200 ml). The organic solution is dried, filtered through celite and evaporated, and the residue is chromatographed on silica gel, eluting with hexane:ethyl acetate, to afford methyl (E) 6-(1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate. B. Methyl (E) 6-(1,3-dihydro-6-hydroxymethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate Methyl (E) 6-(1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate (0.5 g) is dissolved in trifluoroacetic acid (10 ml) at 0° C. After 30 minutes the solvent is removed under vacuum and the residue is chromatographed on silica gel, eluting with hexane:ethyl acetate, to afford methyl (E) 6-(1,3-dihydro-6-hydroxymethyl-7-methyl-3-oxo-4-p-toluenesulfonyl-oxyisobenzofuran-5-yl)-4-methyl-4-hexenoate.

9C. Methyl (E) 6-(.1,.3-.dihydro-6-formyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate

Methyl (E) 6-(1,3-dihydro-6-hydroxymethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate (0.2 g) is dissolved in dichloromethane (10 ml) and pyridinium chlorochromate (0.15 g) is added. After one hour water (25 ml) is added. The organic solution is dried and evaporated and the residue is chromatographed on silica gel, eluting with hexane:ethyl acetate, to afford methyl (E) 6-(1,3-dihydro-6-formyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate.

9D. Formula A where R⁷ is 4-methoxybenzyloxymethyl, Hydroxymethyl and Formyl

By following the procedures of Examples 5 and 6 and substituting methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate with:

methyl (E) 6-(1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-hydroxymethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(1,3-dihydro-6-formyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate,

there are obtained:

(E) 6-(1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(1,3-dihydro-6-hydroxymethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoic acid; and

(E) 6-(1,3-dihydro-6-formyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

Example 10 Preparation of Compounds of Formula 2

10A. Preparation of 2 where Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, R⁷ is Ethyl, and G is Methoxy

To a 0° C. solution of 4.59 g of methyl (E)-6-(1,3-dihydro-4-hydroxy-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate and 2.22 ml of pyridine in 100 ml of methylene chloride is added 2.55 ml of trifluoromethane sulfonic anhydride dropwise. After 30 minutes, the reaction mixture is poured into 1N aqueous sodium hydrogen sulfate. This mixture is extracted with dichloromethane, and the organic phase further washed with water and brine. The organic phase is dried over magnesium sulfate and concentrated under reduced pressure, to give methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-4-trifluoromethyl sulfonyloxy-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

10B. Preparation of 2, varying R⁷

Similarly, following the procedures of Example 10A above, but replacing methyl (E)-6-(1,3-dihydro-4-hydroxy-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula A, the following intermediates of Formula 2 are prepared:

methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoate; and

methyl (E)-2-{2-[2-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-ethylidene]-cyclopent-1-yl}acetate.

10C. Preparation of 2, varying R⁷

Similarly, following the procedures of Example 10A above, but replacing methyl (E)-6-(1,3-dihydro-4-hydroxy-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula A where Z is a sidechain of Formula ZA, in which G is lower alkoxy, the following exemplary intermediates of Formula 2 are prepared:

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-trifluoromethylsulfonyloxy-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6,7-dimethyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-cyclopropyl-1,3-dihydro-7-methyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-fluorovinyl-7-methyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-trifluoromethylsulfonyloxy-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethynyl-7-methyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(pent-2-ynyl)-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-allyl-1,3-dihydro-7-methyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(1,3-dihydro-6-methoxybenzyloxymethyl-7-methyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate.

10D. Preparation of 2, varying R⁷ and Z

Similarly, following the procedures of Example 10A above, but replacing methyl (E)-6-(1,3-dihydro-4-hydroxy-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula A where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, other intermediates of Formula 2 corresponding to those listed in the tables in Example 1B are prepared.

Example 11 Preparation of Compounds of Formula 3

11A. Preparation of 3 where Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, R⁷ is Ethyl, and G is Methoxy

A nitrogen-flushed mixture of 5.8 g (12.4 mmol) of methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-4-trifluoromethyl-sulfonyloxy-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate, 1.5 g of potassium cyanide, and 1.11 g of tetrakis(triphenylphosphine) palladium in 100 ml of 1,4-dioxane is heated at reflux for 18 hours. Upon cooling, the mixture is partitioned between water and ethyl acetate. The organic phase is washed with water six times, with brine once, and then dried over magnesium sulfate. The solvent is evaporated under reduced pressure and the residue purified by silica gel chromatography, to give methyl (E)-6-(4-cyano-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

11B. Preparation of 3, varying Z

Similarly, following the procedures of Example 11A above, but replacing methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4 trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 2, the following intermediates of Formula 3 are prepared:

methyl (E)-6-(4-cyano-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoate; and

methyl (E)-2-{2-[2-(4-cyano-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-ethylidene]-cyclopent-1-yl}acetate.

11C. Preparation of 3, varying R⁷

Similarly, following the procedures of Example 11A above, but replacing methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoromethylsulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 2 where Z is a sidechain of Formula ZA, in which G is lower alkoxy, the following exemplary intermediates of Formula 3 are prepared:

methyl (E) 6-(4-cyano-1,3-dihydro-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-cyano-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-cyano-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-cyano-6-cyclopropyl-1,3-dihydro-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-cyano-1,3-dihydro-6-fluorovinyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-cyano-1,3-dihydro-7-methyl-3-oxo-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-cyano-1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-cyano-1,3-dihydro-6-ethynyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-cyano-1,3-dihydro-7-methyl-3-oxo-6-(pent-2-ynyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-allyl-4-cyano-1,3-dihydro-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(4-cyano-1,3-dihydro-6-(4-methoxybenzyloxy-methyl)-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

11D. Preparation of 3, varying R⁷ and Z

Similarly, following the procedures of Example 11A above, but replacing methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-4-trifluoromethylsulfonyloxy-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 2 where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, other intermediates of Formula 3 corresponding to those listed in the tables in Example 1B are prepared.

Example 12 Preparation of Compounds of Formula 4

12A. Preparation of 4 where Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, R⁷ is Ethyl, and G is Methoxy

A mixture of 4.0 g of methyl (E)-6-(4-cyano-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate and 1.86 g of sodium hydroxide in 100 ml of 3:2 water:methanol is heated at reflux for 2 hours. The resulting homogenous solution is distilled until 30 ml of distillate is recovered. An additional 0.6 g (15 mmol) of sodium hydroxide is added to the reaction solution and it is refluxed for 2 days. Upon cooling the solution is partitioned between 1N aqueous HCl and ethyl acetate. The organic phase is washed twice with water, once with brine, and then dried over magnesium sulfate. The solvent is evaporated under reduced pressure to give (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

12B. Preparation of 4, varying R⁷ and Z

Similarly, following the procedures of Example 12A above, but replacing methyl (E)-6-(4-cyano-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 3, the following intermediates of Formula 4 are prepared:

(E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoic acid; and

(E)-2-{2-[2-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-ethylidene]-cyclopent-1-yl}acetic acid.

12C. Preparation of 4, varying R⁷

Similarly, following the procedures of Example 12A above, but replacing methyl (E)-6-(4-cyano-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 3 where Z is a sidechain of Formula ZA, in which G is lower alkoxy, the following exemplary intermediates of Formula 4 are prepared:

(E) 6-(4-carboxy-1,3-dihydro-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(4-carboxy-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(4-carboxy-6-cyclopropyl-1,3-dihydro-7-methyl-3-oxisobenzofuran5yl)-4-methyl-4hexenoic acid

(E) 6-(4-carboxy-1,3-dihydro-6-fluorovinyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid

(E) 6-(4-carboxy-1,3-dihydro-7-methyl-3-oxo-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(4-carboxy-1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)isobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(4-carboxy-1,3-dihydro-6-ethynyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(4-carboxy-1,3-dihydro-7-methyl-3-oxo-6-(pent-2-ynyl)isobenzofuran-5-yl)-4-methyl-4-hexenoic acid;

(E) 6-(6-allyl-4-carboxy-1,3-dihydro-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid; and

(E) 6-(4-carboxy-1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

12D. Preparation of 4, varying R⁷ and Z

Similarly, following the procedures of Example 12A above, but replacing methyl (E)-6-(4-cyano-1, 3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 3 where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, other intermediates of Formula 4 corresponding to those listed in the tables in Example 1B are prepared.

Example 13 Preparation of Compounds of Formula 5

13A. Preparation of 5 where Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, and R⁷ is Ethyl and G is Methoxy

A solution of 3.88 g of (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid and 0.2 g of p-toluenesulfonic acid in methanol (60 ml) is stirred at room temperature for 8 hours. The solvent is evaporated under reduced pressure. The residue is dissolved in ethyl acetate, and this solution washed twice with water, once with brine, and dried over magnesium sulfate. The solvent is evaporated under reduced pressure to give methyl (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

13B. Preparation of 5, varying R⁷ and Z

Similarly, following the procedures of Example 13A above, but replacing (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid with other compounds of Formula 4, the following intermediates of Formula 5 are prepared:

methyl (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoate; and

methyl (E)-2-{2-[2-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-ethylidene]-cyclopent-1-yl}acetate.

13C. Preparation of 5, varying R⁷

Similarly, following the procedures of Example 13A above, but replacing (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid with other compounds of Formula 4 where Z is a sidechain of Formula ZA, in which G is lower alkoxy, the following exemplary intermediates of Formula 5 are prepared:

methyl (E) 6-(4-carboxy-1,3-dihydro-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-carboxy-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-carboxy-6-cyclopropyl-1,3-dihydro-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-carboxy-1,3-dihydro-6-fluorovinyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-carboxy-1,3-dihydro-7-methyl-3-oxo-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-carboxy-1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-carboxy-1,3-dihydro-6-ethynyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(4-carboxy-1,3-dihydro-7-methyl-3-oxo-6-(pent-2-ynyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-allyl-4-carboxy-1,3-dihydro-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(4-carboxy-1,3-dihydro-6-(4-methoxybenzyloxy-methyl)-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

13D. Preparation of 5, varying R⁷ and Z

Similarly, following the procedures of Example 13A above, but replacing (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid with other compounds of Formula 4 where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, other intermediates of Formula 5 corresponding to those listed in the tables in Example 1B are prepared.

Example 14 Preparation of Compounds of Formula 6

14A. Preparation of 6 where Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, and R⁷ is Ethyl and G is Methoxy

To a stirred, 0° C. solution of 6.0 g of methyl (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate in 150 ml of dimethylformamide is added 4.62 ml of triethylamine followed by dropwise addition of 4.5 ml of diphenylchlorophosphate. The mixture is allowed to stir at room temperature for 1 hour and then recooled to 0° C., and treated with 10.8 g of sodium azide. This mixture is stirred for 24 hours at 0° C. and then partitioned between aqueous sodium hydrogen sulfate and ethyl acetate. The organic phase is washed four times with water, dried over magnesium sulfate, and concentrated under reduced pressure to give methyl (E)-6-(1,3-dihydro-6-ethyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

14B. Preparation of 6, varying R⁷ and Z

Similarly, following the procedures of Example 14A above, but replacing methyl (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 5, the following intermediates of Formula 6 are prepared:

methyl (E)-6-(1,3-dihydro-6-ethyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoate; and

methyl (E)-2-{2-[2-(1,3-dihydro-6-ethyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-ethylidene]-cyclopent-1-yl}acetate.

14C. Preparation of 6, varying R⁷

Similarly, following the procedures of Example 14A above, but replacing methyl (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 5 where Z is a sidechain of Formula ZA, in which G is lower alkoxy, the following exemplary intermediates of Formula 6 are prepared:

methyl (E) 6-(1,3-dihydro-4-isocyanato-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6,7-dimethyl-4-isocyanato-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-cyclopropyl-1,3-dihydro-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-fluorovinyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-4-isocyanato-7-methyl-3-oxo-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-4-isocyanato-7-methyl-3-oxo-6-(prop-2-enyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethynyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-4-isocyanato-7-methyl-3-oxo-6-(pent-2-ynyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-allyl-1,3-dihydro-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(1,3-dihydro-4-isocyanato-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

14D. Preparation of 6, varying R⁷ and Z

Similarly, following the procedures of Example 14A above, but replacing (E)-6-(4-carboxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid with other compounds of Formula 5 where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, other intermediates of Formula 6 corresponding to those listed in the tables in Example 1B are prepared.

Example 15 Preparation of Compounds of Formula I

15A. Formula IA where Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, and R⁷ is Ethyl and G is Hydroxy

2.0 g of methyl (E)-6-(1,3-dihydro-6-ethyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate is dissolved in 50 ml of 1,4-dioxane and treated with 16 ml of water and 2.0 g of lithium hydroxide monohydrate. The mixture is stirred at room temperature for 2 hours and then partitioned between aqueous 1N sodium hydrogen sulfate and ethyl acetate. The organic phase is washed twice with water, once with brine, and dried over magnesium sulfate. The solvent is evaporated under reduced pressure and the residue purified by chromatography on silica gel, to give (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

15B. Preparation of IA, varying R⁷ and Z

Similarly, following the procedures of Example 15A above, but replacing methyl (E)-6-(1,3-dihydro-6-ethyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 6, the following intermediates of Formula IA are prepared:

(E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoic acid; and

(E)-2-{2-[2-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-ethylidene]-cyclopent-1-yl}acetic acid.

15C. Preparation of IA, varying R⁷

Similarly, following the procedures of Example 14A above, but replacing methyl (E)-6-(1,3-dihydro-6-ethyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 6 where Z is a sidechain of Formula ZA, in which G is lower alkoxy, the following exemplary intermediates of Formula 6 are prepared:

(E) 6-(4-amino-1,3-dihydro-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(4-amino-1,3-dihydro-6,7-dimethyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(4-amino-6-cyclopropyl-1,3-dihydro-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(4-amino-1,3-dihydro-6-fluorovinyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(4-amino-1,3-dihydro-7-methyl-3-oxo-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(4-amino-1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(4-amino-1,3-dihydro-6-ethynyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(4-amino-1,3-dihydro-7-methyl-3-oxo-6-(pent-2-ynyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(6-allyl-4-amino-1,3-dihydro-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

(E) 6-(4-amino-1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

15D. Preparation of IA, varying R⁷ and Z

Similarly, following the procedures of Example 15A above, but replacing methyl (E)-6-(1,3-dihydro-6-ethyl-4-isocyanato-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 6 where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, the following compounds of Formula IA where G is hydroxy and R⁷ is ethyl are prepared:

    ______________________________________                                          ##STR84##                                                                     Formula IA where Z is Sidechain ZA                                             Z.sup.1     Z.sup.2   Z.sup.3     Z.sup.4                                      ______________________________________                                         Ethyl       H         H           Methyl                                       n-Propyl    H         H           Methyl                                       CF.sub.3    H         H           Methyl                                       H           H         H           Methyl                                       H           Methyl    H           Methyl                                       Methyl      Methyl    H           Methyl                                       Methyl      Ethyl     H           H                                            Methyl      H         H           Ethyl                                        Methyl      H         H           n-Propyl                                     Methyl      H         Phenyl      H                                            Methyl      H         Phenyl      Methyl                                       Methyl      H         Methoxy     H                                            Methyl      H         Ethoxy      Ethyl                                        Methyl      H         Methylthio  H                                            Methyl      H         Ethylthio   Methyl                                       Methyl      H         Cyclopropyl                                              Methyl      Methyl    H           H                                            ______________________________________                                    

    ______________________________________                                          ##STR85##                                                                     Formula IA where Z is Sidechain ZB                                             D.sup.1 -D.sup.2 Z.sup.5     Z.sup.8                                           ______________________________________                                         (CH.sub.2).sub.2 H           H                                                 (CH.sub.2).sub.4 H           H                                                 (CH.sub.2).sub.5 H           H                                                 ______________________________________                                    

    ______________________________________                                          ##STR86##                                                                     Formula IA where Z is Sidechain ZB                                             D.sup.1 -D.sup.2  Z.sup.5     Z.sup.8                                          ______________________________________                                         CH.sub.2 OCH.sub.2                                                                               H           H                                                (CH.sub.2).sub.2 OCH.sub.2                                                                       H           H                                                CH.sub.2 SCH.sub.2                                                                               H           Methyl                                           CH.sub.2 NHCH.sub.2                                                                              H           H                                                (CH.sub.2).sub.2 OCH.sub.2                                                                       H           Methyl                                           (CH.sub.2).sub.3 OCH.sub.2                                                                       H           H                                                (CH.sub.2).sub.2  Methyl      H                                                (CH.sub.2).sub.3  Methyl      H                                                (CH.sub.2).sub.3  Ethyl       H                                                (CH.sub.2).sub.3  n-Propyl    H                                                (CH.sub.2).sub.4  Methyl      H                                                (CH.sub.2).sub.4  Ethyl       Methyl                                           (CH.sub.2).sub.3  n-Hexyl     Methyl                                           ______________________________________                                    

    ______________________________________                                          ##STR87##                                                                     Formula IA where Z is Sidechain ZE                                             Z.sup.5      Z.sup.6       Z.sup.7                                             ______________________________________                                         H            H             H                                                   H            3-Methyl      H                                                   H            6-Methyl      H                                                   H            5-t-Butyl     H                                                   H            5-Methyl      6-Methyl                                            H            5-Methoxy     H                                                   ______________________________________                                    

    ______________________________________                                          ##STR88##                                                                     Formula IA where Z is Sidechain ZE                                             Z.sup.5       Z.sup.6       Z.sup.7                                            ______________________________________                                         H             4-COOH        H                                                  H             4-Chloro      H                                                  H             5-Chloro      H                                                  H             5-Bromo       6-Bromo                                            H             5-Nitro       H                                                  H             6-Nitro       H                                                  Methyl        3-Methyl      H                                                  Methyl        6-Methyl      H                                                  Methyl        5-t-Butyl     H                                                  Methyl        5-Methyl      6-Methyl                                           Methyl        5-Methoxy     H                                                  Methyl        4-COOH        H                                                  Methyl        4-Chloro      H                                                  Methyl        5-Chloro      H                                                  Methyl        5-Bromo       6-Bromo                                            Methyl        6-Nitro       H                                                  n-Propyl      H             H                                                  n-Propyl      3-Methyl      H                                                  n-Propyl      6-Methyl      H                                                  n-Propyl      5-t-Butyl     H                                                  n-Propyl      5-Methyl      6-Methyl                                           n-Propyl      5-Methoxy     H                                                  n-Propyl      4-COOH        H                                                  n-Propyl      4-Chloro      H                                                  n-Propyl      5-Chloro      H                                                  n-Propyl      5-Bromo       6-Bromo                                            n-Propyl      6-Nitro       H                                                  ______________________________________                                    

    ______________________________________                                          ##STR89##                                                                     Formula IA where Z is                                                          Sidechain ZH                                                                          D.sup.4       Z.sup.1                                                   ______________________________________                                                CH.sub.2      Methyl                                                           OCH.sub.2     Methyl                                                           CH.sub.2      Ethyl                                                            CH.sub.2      n-Propyl                                                         (CH.sub.2).sub.2                                                                             H                                                                (CH.sub.2).sub.2                                                                             Methyl                                                           (CH.sub.2).sub.2                                                                             Ethyl                                                            (CH.sub.2).sub.3                                                                             H                                                                (CH.sub.2).sub.3                                                                             Methyl                                                           CH.sub.2      CF.sub.3                                                  ______________________________________                                    

Example 16 Preparation of Compounds of Formula I

16A. Formula IA where Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, R⁷ is Ethyl, and G is Methoxy

To a solution of 2.5 g of (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid in 50 ml (1.234 mol) of methanol is added 0.125 g of p-toluenesulfonic acid monohydrate. The solution is stirred at room temperature for 2 days and then concentrated to a small volume, and the residue partitioned between water and ethyl acetate. The organic layer is dried over magnesium sulfate and concentrated to give methyl (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

16B. Preparation of IA, varying Z in which G is Lower Alkoxy

Similarly, following the procedures of Example 16A above, but optionally replacing (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid with other compounds of Formula IA where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is hydroxy, and optionally replacing methanol with other alkanols of formula GH, where G is lower alkoxy, the compounds of Formula IA corresponding to those listed in the tables in Example 15D where G is lower alkoxy are prepared.

Example 17 Preparation of Compounds of Formula I

17A. Formula IA where Z is ZA in which Z¹ is Methyl Z², Z³ and Z⁴ are Hydrogen, R⁷ is Ethyl, and G is Morpholinoethoxy

7 g of (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid and toluene (25 ml) are warmed gently to form a solution. A slight excess of 2-morpholinoethanol (3 g) and toluene (25 ml) are added. The reaction mixture is stirred for half an hour and then heated to reflux at an initial pot temperature of 117° C. (which increases a few degrees during reflux) under a Dean-Stark trap for 80 hours. The reaction mixture is cooled, washed with water (2×15 ml), 10% aqueous sodium bicarbonate (2×15 ml) and finally with water (15 ml). The toluene layer is stripped to a volume of about 20 ml in vacuo, n-hexane (30 ml) is added and the resulting slurry is aged at room temperature for 2 hours. The product is filtered, washed with n-hexane (ca. 10 ml) and dried in vacuo at 60° C. to yield 2-(morpholin-4-yl)ethyl (E)-6 -(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

17B. Preparation of IA varying Z in which G is Morpholinoethoxy

Similarly, following the procedures of Example 17A above, but replacing (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid with other compounds of Formula IA where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is hydroxy, the corresponding compounds of Formula IA where G is morpholinoethoxy are prepared.

Example 18 Preparation of Compounds of Formula I

18A. Formula IB where R⁴ and R⁵ are Methyl, R⁷ is Ethyl, and Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, and G is Methoxy

A solution of 0.65 g (1.8 mmol) of methyl (E)-6-(1,3-dihydro-4-isocyanato-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate in 10 ml of tetrahydrofuran is treated with 5 ml of a solution of 40% dimethylamine in water. After 1 hour the reaction is partitioned between water and ethyl acetate. The organic phase is washed with water three times, dried over magnesium sulfate, and concentrated under reduced pressure to give methyl (E)-6-[1,3-dihydro-4-(3,3-dimethylureido)-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate.

18B. Preparation of IB, varying Z

Similarly, following the procedures of Example 18A above, but replacing methyl (E)-6-(1,3-dihydro-4-isocyanato-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula 6 where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, the corresponding compounds of Formula IB where G is lower alkoxy are prepared.

Example 19 Preparation of Compounds of Formula I

19A. Formula IB where R⁴ and R⁵ are Methyl, R⁷ is Ethyl, and Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, and G is Hydroxy

To a solution of 0.3 g (0.74 mmol) of methyl (E)-6-[1,3-dihydro-4-(3,3-dimethylureido)-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate in 7.4 ml of 4:1 methanol:water is added 0.13 g (2.96 mmol) of lithium hydroxide monohydrate. The solution is heated at 50°-60° C. for 4 hours. Upon cooling, the reaction is partitioned between aqueous sodium hydrogen sulfate and ethyl acetate. The organic layer is washed with brine, dried over magnesium sulfate, and concentrated to give (E)-6-[1,3-dihydro-4-(3,3-dimethylureido)-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoic acid.

19B. Preparation of IB, varying R⁴, R⁵, R⁷, and Z in which G is Hydroxy

Similarly, following the procedures of Example 19A above, but replacing methyl (E)-6-[1,3-dihydro-4-(3,3-dimethylureido)-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate with other compounds of Formula IB in which G is lower alkoxy, the following exemplary intermediates of Formula IB where G is hydroxy are prepared:

(E)-6-(1,3-dihydro-4-(3,3-dimethylureido)-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoic acid;

(E)-2-{2-[2-(1,3-dihydro-4-(3,3-dimethylureido)-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-ethylidene]-cyclopent-1-yl}acetic acid;

(E) 6-(1,3-dihydro-4-(3,3-dimethylureido)-7-methyl-3-oxo-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(1,3-dihydro-6,7-dimethyl-4-(3,3-dimethylureido)-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(1,3-dihydro-4-(3,3-dimethylureido)-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(6-cyclopropyl-1,3-dihydro-4-(3,3-dimethylureido)-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(1,3-dihydro-4-(3,3-dimethylureido)-6-fluorovinyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(1,3-dihydro-4-(3,3-dimethylureido)-7-methyl-3-oxo-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(1,3-dihydro-4-(3,3-dimethylureido)-7-methyl-3-oxo-6-(prop-2-enyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(1,3-dihydro-4-(3,3-dimethylureido)-6-ethynyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(1,3-dihydro-4-(3,3-dimethylureido)-7-methyl-3-oxo-6-(pent-2-ynyl)isobenzofuran-5-yl)-4-methyl-4-hexenoate;

(E) 6-(6-allyl-1,3-dihydro-4-(3,3-dimethylureido)-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

(E) 6-(1,3-dihydro-4-(3,3-dimethylureido)-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

19C. Preparation of IB, varying Z

Similarly, following the procedures of Example 18A and 19A above, but replacing methyl (E)-6-[1,3-dihydro-4-(3,3-dimethylureido)-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate with other compounds of Formula IB where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, the following compounds of Formula IB where G is hydroxy and R⁷ is ethyl are prepared:

    ______________________________________                                          ##STR90##                                                                     Formula IB where Z is Sidechain ZA                                             R.sup.4                                                                               R.sup.5   Z.sup.1   Z.sup.2                                                                               Z.sup.3                                                                              Z.sup.4                                ______________________________________                                         H      H         Ethyl     H      H     Methyl                                 H      H         n-Propyl  H      H     Methyl                                 H      H         CF.sub.3  H      H     Methyl                                 H      Methyl    H         H      H     Methyl                                 H      Methyl    H         Methyl H     Methyl                                 H      Methyl    Methyl    Methyl H     Methyl                                 ______________________________________                                    

    ______________________________________                                          ##STR91##                                                                     Formula IB where Z is Sidechain ZA                                             R.sup.4                                                                               R.sup.5 Z.sup.1  Z.sup.2                                                                               Z.sup.3 Z.sup.4                                 ______________________________________                                         H      Methyl  Methyl   H      H       Methyl                                  H      Methyl  Methyl   H      H       Ethyl                                   Methyl Methyl  Methyl   H      H       n-Propyl                                H      H       Methyl   Ethyl  H       H                                       H      H       Methyl   H      Phenyl  Methyl                                  H      Methyl  Methyl   H      Methoxy H                                       H      Methyl  Methyl   H      Ethoxy  Ethyl                                   H      Methyl  Methyl   H      CH.sub.3 S                                                                             H                                       H      Methyl  Methyl   H      C.sub.2 H.sub.5 S                                                                      Methyl                                  H      H       Methyl   H      Cyclopropyl                                     H      H       Methyl    Methyl                                                                               H       H                                       ______________________________________                                    

    ______________________________________                                          ##STR92##                                                                     Formula IB where Z is Sidechain ZB                                             D.sup.1 -D.sup.2                                                                             R.sup.4 R.sup.5  Z.sup.5                                                                              Z.sup.8                                   ______________________________________                                         (CH.sub.2).sub.2                                                                             H       H        H     H                                         (CH.sub.2).sub.4                                                                             H       H        H     H                                         (CH.sub.2).sub.5                                                                             H       H        H     H                                         CH.sub.2OCH.sub.2                                                                            H       H        H     H                                         (CH.sub.2).sub.2OCH.sub.2                                                                    H       H        H     H                                         CH.sub.2SCH.sub.2                                                                            H       Methyl   H     Methyl                                    ______________________________________                                    

    ______________________________________                                          ##STR93##                                                                     Formula IB where Z is Sidechain ZB                                             D.sup.1 -D.sup.2                                                                           R.sup.4  R.sup.5  Z.sup.5 Z.sup.8                                  ______________________________________                                         CH.sub.2NHCH.sub.2                                                                         H        Methyl   H       H                                        (CH.sub.2).sub.2OCH.sub.2                                                                  Methyl   Methyl   H       Methyl                                   (CH.sub.2).sub.3OCH.sub.2                                                                  Methyl   Methyl   H       H                                        (CH.sub.2).sub.2                                                                           H        Methyl   Methyl  H                                        (CH.sub.2).sub.3                                                                           H        Methyl   Methyl  H                                        (CH.sub.2).sub.3                                                                           H        Methyl   Ethyl   H                                        (CH.sub.2).sub.3                                                                           H        H        n-Propyl                                                                               H                                        (CH.sub.2).sub.4                                                                           H        H        Methyl  H                                        (CH.sub.2).sub.4                                                                           H        H        Ethyl   Methyl                                   (CH.sub. 2).sub.3                                                                          H        H        n-Hexyl Methyl                                   ______________________________________                                    

    ______________________________________                                          ##STR94##                                                                     Formula IB where Z is Sidechain ZE                                             R.sup.4 R.sup.5   Z.sup.5 Z.sup.6   Z.sup.7                                    ______________________________________                                         H       H         H       H         H                                          H       H         H       3-Methyl  H                                          H       H         H       6-Methyl  H                                          H       H         H       5-t-Butyl H                                          H       Methyl    H       5-Methyl  6-Methyl                                   H       Methyl    H       5-Methoxy H                                          H       H         H       4-COOH    H                                          H       H         H       4-Chloro  H                                          ______________________________________                                    

    ______________________________________                                          ##STR95##                                                                     Formula IB where Z is Sidechain ZE                                             R.sup.4                                                                               R.sup.5   Z.sup.5   Z.sup.6   Z.sup.7                                   ______________________________________                                         H      Methyl    H         5-Chloro  H                                         H      Methyl    H         5-Bromo   6-Bromo                                   H      Methyl    H         5-Nitro   H                                         H      H         H         6-Nitro   H                                         H      H         Methyl    3-Methyl  H                                         H      Methyl    Methyl    6-Methyl  H                                         H      H         Methyl    5-t-Butyl H                                         H      H         Methyl    5-Methyl  6-Methyl                                  H      Methyl    Methyl    5-Methoxy H                                         H      H         Methyl    4-COOH    H                                         H      Methyl    Methyl    4-Chloro  H                                         H      Methyl    Methyl    5-Chloro  H                                         H      H         Methyl    5-Bromo   6-Bromo                                   H      Methyl    Methyl    6-Nitro   H                                         H      H         n-Propyl  H         H                                         H      Methyl    n-Propyl  3-Methyl  H                                         H      H         n-Propyl  6-Methyl  H                                         H      H         n-Propyl  5-t-Butyl H                                         H      H         n-Propyl  5-Methyl  6-Methyl                                  H      H         n-Propyl  5-Methoxy H                                         H      H         n-Propyl  4-COOH    H                                         H      H         n-Propyl  4-Chloro  H                                         H      H         n-Propyl  5-Chloro  H                                         H      H         n-Propyl  5-Bromo   6-Bromo                                   H      H         n-Propyl  6-Nitro   H                                         ______________________________________                                    

    ______________________________________                                          ##STR96##                                                                     Formula IB where Z is Sidechain ZH                                             R.sup.4    R.sup.5    D.sup.4    Z.sup.1                                       ______________________________________                                         H          H          CH.sub.2   Methyl                                        H          H          OCH.sub.2  Methyl                                        H          Methyl     CH.sub.2   Ethyl                                         H          Methyl     CH.sub.2   n-Propyl                                      H          H          (CH.sub.2).sub.2                                                                          H                                             H          Methyl     (CH.sub.2).sub.2                                                                          Methyl                                        H          H          (CH.sub.2).sub.2                                                                          Ethyl                                         H          Methyl     (CH.sub.2).sub.3                                                                          H                                             H          Methyl     (CH.sub.2).sub.3                                                                          Methyl                                        Methyl     Methyl     CH.sub.2   CF.sub.3                                      ______________________________________                                    

Example 20 Preparation of Compounds of Formula I

20A. Formula IC where R³ is --CF₃, and Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, and R⁷ is Ethyl and G is Methoxy

To a solution of 0.5 g of methyl (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate in 5 ml of dichloromethane is added 0.5 ml of trifluoroacetic anhydride. After 1 hour the reaction is partitioned between water and dichloromethane. The organic layer is washed twice with water, dried over magnesium sulfate, and concentrated to give methyl (E)-6-[1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl]-4-methyl-4-hexenoate.

20B. Formula IC where R³ is --CF₃, varying R⁷ and Z

Similarly, following the procedures of Example 20A above, but replacing methyl (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula IA in which G is lower alkoxy, the following exemplary intermediates of Formula IC where G is lower alkoxy are prepared:

methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoic acid;

methyl (E)-2-{2-[2-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-ethylidene]-cyclopent-1-yl}acetic acid;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-trifluoroacetylamino-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6,7-dimethyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-cyclopropyl-1,3-dihydro-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-fluorovinyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-trifluoroacetylamino-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)-4-trifluoroacetylaminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethynyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(pent-2-ynyl)-4-trifluoroacetylaminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-allyl-1,3-dihydro-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(1,3-dihydro-6-methoxybenzyloxymethyl-7-methyl-3-oxo-4-trifluoroacetylaminoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

20C. Preparation Of IC, varying z

Similarly, following the procedures of Example 20A above, but replacing methyl (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate with other compounds of Formula IA where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, and optionally replacing trifluoroacetic anhydride with other compounds of the formula (R³ C(O))₂ O or of the formula R³ C(O)Cl, where R³ is as defined in the Summary of the Invention, the following compounds of Formula IC where G is hydroxy and R⁷ is ethyl are prepared:

    ______________________________________                                          ##STR97##                                                                     Formula IC where Z is Sidechain ZA                                             R.sup.3 Z.sup.1    Z.sup.2  Z.sup.3  Z.sup.4                                   ______________________________________                                         CF.sub.3                                                                               Ethyl      H        H        Methyl                                    CF.sub.3                                                                               n-Propyl   H        H        Methyl                                    CF.sub.3                                                                               CF.sub.3   H        H        Methyl                                    CF.sub.3                                                                               H          H        H        Methyl                                    CF.sub.3                                                                               H          Methyl   H        Methyl                                    CF.sub.3                                                                               Methyl     Methyl   H        Methyl                                    CF.sub.3                                                                               Methyl     Ethyl    H        H                                         CF.sub.3                                                                               Methyl     H        H        Ethyl                                     CF.sub.3                                                                               Methyl     H        H        n-Propyl                                  CH.sub.3                                                                               Methyl     H        Phenyl   H                                         CF.sub.3                                                                               Methyl     H        Phenyl   Methyl                                    CF.sub.3                                                                               Methyl     H        Methoxy  H                                         CF.sub.3                                                                               Methyl     H        Ethoxy   Ethyl                                     CF.sub.3                                                                               Methyl     H        CH.sub.3 S                                                                              H                                         CF.sub.3                                                                               Methyl     H        C.sub.2 H.sub.5 S                                                                       Methyl                                    CF.sub.3                                                                               Methyl     H        Cyclopropyl                                        H       Methyl     Methyl   H        H                                         ______________________________________                                    

    ______________________________________                                          ##STR98##                                                                     Formula IC where Z is Sidechain ZB                                             D.sup.1 -D.sup.2                                                                             R.sup.3    Z.sup.5   Z.sup.8                                     ______________________________________                                         (CH.sub.2).sub.2                                                                             CF.sub.3   H         H                                           (CH.sub.2).sub.4                                                                             CF.sub.3   H         H                                           (CH.sub.2).sub.5                                                                             CF.sub.3   H         H                                           CH.sub.2OCH.sub.2                                                                            CF.sub.3   H         H                                           (CH.sub.2).sub.2OCH.sub.2                                                                    CF.sub.3   H         H                                           CH.sub.2SCH.sub.2                                                                            CF.sub.3   H         Methyl                                      CH.sub.2NHCH.sub.2                                                                           Methyl     H         H                                           (CH.sub.2).sub.2OCH.sub.2                                                                    Ethyl      H         Methyl                                      (CH.sub.2).sub.3OCH.sub.2                                                                    Ethyl      H         H                                           (CH.sub.2).sub. 2                                                                            n-Propyl   Methyl    H                                           (CH.sub.2).sub.3                                                                             Hexyl      Methyl    H                                           (CH.sub.2).sub.3                                                                             CHF.sub.2  Ethyl     H                                           (CH.sub.2).sub.3                                                                             CH.sub.2 F n-Propyl  H                                           (CH.sub.2).sub.4                                                                             CF.sub.3   Methyl    H                                           (CH.sub.2).sub.4                                                                             CF.sub.3   Ethyl     Methyl                                      (CH.sub.2).sub.3                                                                             CF.sub.3   n-Hexyl   Methyl                                      ______________________________________                                    

    ______________________________________                                          ##STR99##                                                                     Formula IC where Z is Sidechain ZE                                             R.sup.3       Z.sup.5   Z.sup.6    Z.sup.7                                     ______________________________________                                         CF.sub.3      H         H          H                                           ______________________________________                                    

    ______________________________________                                          ##STR100##                                                                    Formula IC where Z is Sidechain ZE                                             R.sup.3    Z.sup.5    Z.sup.6     Z.sup.7                                      ______________________________________                                         CF.sub.3   H          3-Methyl    H                                            CF.sub.3   H          6-Methyl    H                                            CF.sub.3   H          5-t-Butyl   H                                            CF.sub.3   H          5-Methyl    6-Methyl                                     CF.sub.3   H          5-Methoxy   H                                            Methyl     H          4-COOH      H                                            Ethyl      H          4-Chloro    H                                            n-Propyl   H          5-Chloro    H                                            CHF.sub.2  H          5-Bromo     6-Bromo                                      CH.sub.2 F H          5-Nitro     H                                            CF.sub.3   H          6-Nitro     H                                            H          Methyl     3-Methyl    H                                            CH.sub.3   Methyl     6-Methyl    H                                            CF.sub.3   Methyl     5-t-Butyl   H                                            CF.sub.3   Methyl     5-Methyl    6-Methyl                                     CF.sub.3   Methyl     5-Methoxy   H                                            CF.sub.3   Methyl     4-COOH      H                                            CF.sub.3   Methyl     4-Chloro    H                                            CF.sub.3   Methyl     5-Chloro    H                                            CF.sub. 3  Methyl     5-Bromo     6-Bromo                                      CF.sub.3   Methyl     6-Nitro     H                                            CF.sub.3   n-Propyl   H           H                                            CF.sub.3   n-Propyl   3-Methyl    H                                            CF.sub.3   n-Propyl   6-Methyl    H                                            CF.sub.3   n-Propyl   5-t-Butyl   H                                            CF.sub.3   n-Propyl   5-Methyl    6-Methyl                                     CF.sub.3   n-Propyl   5-Methoxy   H                                            ______________________________________                                    

    ______________________________________                                          ##STR101##                                                                    Formula IC where Z is Sidechain ZE                                             R.sup.3   Z.sup.5     Z.sup.6    Z.sup.7                                       ______________________________________                                         CF.sub.3  n-Propyl    4-COOH     H                                             CF.sub.3  n-Propyl    4-Chloro   H                                             CF.sub.3  n-Propyl    5-Chloro   H                                             CF.sub.3  n-Propyl    5-Bromo    6-Bromo                                       CF.sub.3  n-Propyl    6-Nitro    H                                             ______________________________________                                    

    ______________________________________                                          ##STR102##                                                                    Formula IC where Z is Sidechain ZH                                             R.sup.3        D.sup.4      Z.sup.1                                            ______________________________________                                         CF.sub.3       CH.sub.2     Methyl                                             CF.sub.3       OCH.sub.2    Methyl                                             CF.sub.3       CH.sub.2     Ethyl                                              CF.sub.3       CH.sub.2     n-Propyl                                           CF.sub.3       (CH.sub.2).sub.2                                                                            H                                                  CF.sub.3       (CH.sub.2).sub.2                                                                            Methyl                                             Methyl         (CH.sub.2).sub.2                                                                            Ethyl                                              Ethyl          (CH.sub.2).sub.3                                                                            H                                                  CHF.sub.2      (CH.sub.2).sub.3                                                                            Methyl                                             CH.sub.2 F     CH.sub.2     CF.sub.3                                           ______________________________________                                    

Example 21 Preparation of Compounds of Formula I

21. Formula ID where R¹ is Methyl, R³ is --CF₃, R⁷ is Ethyl, and Z is ZA, in which Z¹ is Methyl, Z², Z³, and Z⁴ are Hydrogen, and G is Methoxy

To a solution of 0.35 g of methyl (E)-6-[1,3-dihydro-6-ethyl-7-methyl-4-trifluoroacetylamino-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate in 4 ml of dimethylformamide is added 0.47 g of potassium carbonate and 0.23 ml of iodomethane. The mixture is stirred for 24 hours and then partitioned between ethyl acetate and water. The organic layer is washed with water, dried over magnesium sulfate, and concentrated under reduced pressure to give methyl (E)-6-[1,3-dihydro-6-ethyl-7-methyl-4-(N-trifluoroacetyl-N-methyl)amino-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate.

21B. Formula ID where R³ is --CF₃, varying R⁷ and Z

Similarly, following the procedures of Example 21A above, but replacing methyl (E)-6-[1,3-dihydro-6-ethyl-7-methyl-4-trifluoroacetylamino-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate with other compounds of Formula IC in which G is lower alkoxy, the following exemplary intermediates of Formula ID where U is lower alkoxy are prepared:

methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoic acid;

methyl (E)-2-{2-[2-(1,3-dihydro-6-ethyl-7-methyl-4-(N-trifluoroacetyl-N-methyl)amino-3-oxoisobenzofuran-5-yl)-ethylidene]-cyclopont-1-yl}acetic acid;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)amino-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6,7-dimethyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-cyclopropyl-1,3-dihydro-7-methyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-fluorovinyl-7-methyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)amino-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(prop-2-enyl)-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethynyl-7-methyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-6-(pent-2-ynyl)-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-allyl-1,3-dihydro-7-methyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-3-oxo-4-(N-trifluoroacetyl-N-methyl)aminoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

21C. Preparation of ID, varying Z

Similarly, following the procedures of Example 21A above, but replacing methyl (E)-6-[1,3-dihydro-6-ethyl-7-methyl-4-trifluoroacetylamino-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate with other compounds of Formula IC where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, and optionally replacing iodomethane by other lower alkyl halides of the formula R¹ Br or R¹ I, the following compounds of Formula ID where G is hydroxy and R^(v) is ethyl are prepared:

    ______________________________________                                          ##STR103##                                                                    Formula ID where Z is Sidechain ZA                                             R.sup.1                                                                               R.sup.3   Z.sup.1   Z.sup.2                                                                               Z.sup.3                                                                             Z.sup.4                                 ______________________________________                                         Methyl CF.sub.3  Ethyl     H      H    Methyl                                  Methyl CF.sub.3  n-Propyl  H      H    Methyl                                  Methyl CF.sub.3  CF.sub.3  H      H    Methyl                                  Methyl CF.sub.3  H         H      H    Methyl                                  Methyl CF.sub.3  H         Methyl H    Methyl                                  Methyl CF.sub.3  Methyl    Methyl H    Methyl                                  Methyl Methyl    Methyl    Ethyl  H    H                                       Methyl Ethyl     Methyl    H      H    Ethyl                                   Methyl n-Propyl  Methyl    H      H    n-Propyl                                ______________________________________                                    

    ______________________________________                                          ##STR104##                                                                    Formula ID where Z is Sidechain ZA                                             R.sup.1 R.sup.3  Z.sup.1  Z.sup.2                                                                               Z.sup.3 Z.sup.4                               ______________________________________                                         n-Propyl                                                                               CH.sub.2 F                                                                              Methyl   H      Phenyl  H                                     N-Butyl CF.sub.3 Methyl   H      Phenyl  Methyl                                Methyl  CF.sub.3 Methyl   H      Methoxy H                                     Methyl  CF.sub.3 Methyl   H      Ethoxy  Ethyl                                 Methyl  CF.sub.3 Methyl   H      CH.sub.3 S                                                                             H                                     Methyl  CF.sub.3 Methyl   H      C.sub.2 H.sub.5 S                                                                      Methyl                                Methyl  CF.sub.3 Methyl   H      Cyclopropyl                                   Methyl  H        Methyl   Methyl H       H                                     ______________________________________                                    

    ______________________________________                                          ##STR105##                                                                    Formula ID where Z is Sidechain ZB                                             D.sup.1 -D.sup.2                                                                             R.sup.1  R.sup.3  Z.sup.5                                                                              Z.sup.8                                  ______________________________________                                         (CH.sub.2).sub.2                                                                             Methyl   CF.sub.3 H     H                                        (CH.sub.2).sub.4                                                                             Methyl   CF.sub.3 H     H                                        (CH.sub.2).sub.5                                                                             Methyl   CF.sub.3 H     H                                        CH.sub.2OCH.sub.2                                                                            Methyl   CF.sub.3 H     H                                        (CH.sub.2).sub.2OCH.sub.2                                                                    Methyl   CF.sub.3 H     H                                        CH.sub.2SCH.sub.2                                                                            Methyl   CF.sub.3 H     Methyl                                   CH.sub.2NHCH.sub.2                                                                           Methyl   Methyl   H     H                                        (CH.sub.2).sub.2OCH.sub.2                                                                    Methyl   Ethyl    H     Methyl                                   (CH.sub.2).sub.3OCH.sub. 2                                                                   Methyl   Ethyl    H     H                                        ______________________________________                                    

    ______________________________________                                          ##STR106##                                                                    Formula ID where Z is Sidechain ZB                                             D.sup.1 -D.sup.2                                                                        R.sup.1   R.sup.3    Z.sup.5 Z.sup.8                                  ______________________________________                                         (CH.sub.2).sub.2                                                                        Ethyl     n-Propyl   Methyl  H                                        (CH.sub.2).sub.3                                                                        n-Propyl  t-Butyl    Methyl  H                                        (CH.sub.2).sub.3                                                                        n-Butyl   CHF.sub.2  Ethyl   H                                        (CH.sub.2).sub.3                                                                        Methyl    CH.sub.2 F n-Propyl                                                                               H                                        (CH.sub.2).sub.4                                                                        Methyl    CF.sub.3   Methyl  H                                        (CH.sub.2).sub.4                                                                        Methyl    CF.sub.3   Ethyl   Methyl                                   (CH.sub.2).sub.3                                                                        Methyl    CF.sub.3   n-Hexyl Methyl                                   ______________________________________                                    

    ______________________________________                                          ##STR107##                                                                    Formula ID where Z is Sidechain ZE                                             R.sup.1  R.sup.3    Z.sup.5                                                                               Z.sup.6   Z.sup.7                                   ______________________________________                                         Methyl   CF.sub.3   H      H         H                                         Methyl   CF.sub.3   H      3-Methyl  H                                         Methyl   CF.sub.3   H      6-Methyl  H                                         Methyl   CF.sub.3   H      5-t-Butyl H                                         Methyl   CF.sub.3   H      5-Methyl  6-Methyl                                  Methyl   CF.sub.3   H      5-Methoxy H                                         Methyl   Methyl     H      4-COOH    H                                         Methyl   Ethyl      H      4-Chloro  H                                         Methyl   Ethyl      H      5-Chloro  H                                         Ethyl    n-Propyl   H      5-Bromo   6-Bromo                                   ______________________________________                                    

    ______________________________________                                          ##STR108##                                                                    Formula ID where Z is Sidechain ZE                                             R.sup.1 R.sup.3   Z.sup.5   Z.sup.6  Z.sup.7                                   ______________________________________                                         n-Propyl                                                                               t-Butyl   H         5-Nitro  H                                         n-Butyl n-Hexyl   H         6-Nitro  H                                         Methyl  CH.sub.2 F                                                                               Methyl    3-Methyl H                                         Methyl  CHF.sub.2 Methyl    6-Methyl H                                         Methyl  CF.sub.3  Methyl    5-t-Butyl                                                                               H                                         Methyl  CF.sub.3  Methyl    5-Methyl 6-Methyl                                  Methyl  CF.sub.3  Methyl    5-Methoxy                                                                               H                                         Methyl  CF.sub.3  Methyl    4-COOH   H                                         Methyl  CF.sub.3  Methyl    4-Chloro H                                         Methyl  CF.sub.3  Methyl    5-Chloro H                                         Methyl  CF.sub.3  Methyl    5-Bromo  6-Bromo                                   Methyl  CF.sub.3  Methyl    6-Nitro  H                                         Methyl  CF.sub.3  n-Propyl  H        H                                         Methyl  CF.sub.3  n-Propyl  3-Methyl H                                         Methyl  CF.sub.3  n-Propyl  6-Methyl H                                         Methyl  CF.sub.3  n-Propyl  5-t-Butyl                                                                               H                                         Methyl  CF.sub.3  n-Propyl  5-Methyl 6-Methyl                                  Methyl  CF.sub.3  n-Propyl  5-Methoxy                                                                               H                                         Methyl  CF.sub.3  n-Propyl  4-COOH   H                                         Methyl  CF.sub.3  n-Propyl  4-Chloro H                                         Methyl  CF.sub.3  n-Propyl  5-Chloro H                                         Methyl  CF.sub.3  n-Propyl  5-Bromo  6-Bromo                                   Methyl  CF.sub.3  n-Propyl  6-Nitro  H                                         ______________________________________                                    

    ______________________________________                                          ##STR109##                                                                    Formula ID where Z is Sidechain ZH                                             R.sup.1     R.sup.3   D.sup.4     Z.sup.1                                      ______________________________________                                         Methyl      CF.sub.3  CH.sub.2    Methyl                                       Methyl      CF.sub.3  OCH.sub.2   Methyl                                       Methyl      CF.sub.3  CH.sub.2    Ethyl                                        Methyl      CF.sub.3  CH.sub.2    n-Propyl                                     Ethyl       CF.sub.3  (CH.sub.2).sub.2                                                                           H                                            n-Propyl    CF.sub.3  (CH.sub.2).sub.2                                                                           Methyl                                       N-Butyl     Methyl    (CH.sub.2).sub.2                                                                           Ethyl                                        Methyl      Ethyl     (CH.sub.2).sub.3                                                                           H                                            Methyl      CHF.sub.2 (CH.sub.2).sub.3                                                                           Methyl                                       Methyl      CH.sub.2 F                                                                               CH.sub.2    CF.sub.3                                     ______________________________________                                    

Example 22 preparation of Compounds of Formula I

22A. Formula IE where R¹ is Methyl, R⁷ is Ethyl, and Z is ZA, in which Z¹ is Methyl, Z², Z³, Z⁴ are Hydrogen and G is Hydroxy

Hydrolysis of methyl (E)-6-[1,3-dihydro-6-ethyl-7-methyl-4-(N-trifluoroacetyl-N-methyl)amino-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate is carried on the same manner as shown in Example 19A to give methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

22B. Formula IE where R³ is --CF₃, varying R⁷ and Z

Similarly, following the procedures of Example 22A above, but replacing methyl (E)-6-[1,3-dihydro-6-ethyl-7-methyl-4-(N-trifluoroacetyl-N-methyl)amino-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate with other compounds of Formula ID in which G is lower alkoxy, the following exemplary intermediates of Formula IE where G is lower alkoxy are prepared:

methyl (E)-6-(1,3-dihydro-6-ethyl-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)-3,4-dimethyl-4-hexenoic acids;

methyl (E)-2-{2-[2-(1,3-dihydro-6-ethyl-7-methyl-4-methylamino-3-oxoisobenzofuran-5-y 1)-ethylidene]-cyclopent-1-yl}acetic acid;

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-methylamino-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6,7-dimethyl-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethyl-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-cyclopropyl-1,3-dihydro-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-fluorovinyl-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-4-methylamino-3-oxo-6-trifluorovinylisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-6-(prop-2-enyl)-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-6-ethynyl-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(1,3-dihydro-7-methyl-6-(pent-2-ynyl)-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate;

methyl (E) 6-(6-allyl-1,3-dihydro-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate; and

methyl (E) 6-(1,3-dihydro-6-(4-methoxybenzyloxymethyl)-7-methyl-4-methylamino-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

preparation of IE, varying Z

Similarly, following the procedures of Example 22A above, but replacing methyl (E)-6-[1,3-dihydro-6-ethyl-7-methyl-4-(N-trifluoroacetyl-N-methyl)amino-3-oxoisobenzofuran-5-yl]-4-methyl-4-hexenoate with other compounds of Formula ID where Z is a sidechain of Formula ZA, ZB, ZC, ZD, ZE, ZF. ZG, or ZH, in which G is lower alkoxy, the following compounds of Formula IE where G is hydroxy and R⁷ is ethyl are prepared:

    ______________________________________                                          ##STR110##                                                                    Formula IE where Z is Sidechain ZA                                             R.sup.1   Z.sup.1   Z.sup.2  Z.sup.3 Z.sup.4                                   ______________________________________                                         Methyl    Ethyl     H        H       Methyl                                    Methyl    n-Propyl  H        H       Methyl                                    Methyl    CF.sub.3  H        H       Methyl                                    Methyl    H         H        H       Methyl                                    Methyl    H         Methyl   H       Methyl                                    Methyl    Methyl    Methyl   H       Methyl                                    Methyl    Methyl    Ethyl    H       H                                         Methyl    Methyl    H        H       Ethyl                                     Methyl    Methyl    H        H       n-Propyl                                  Methyl    Methyl    H        Cl      H                                         N-Butyl   Methyl    H        Phenyl  Methyl                                    Methyl    Methyl    H        Methoxy H                                         Methyl    Methyl    H        Ethoxy  Ethyl                                     Methyl    Methyl    H        CH.sub.3 S                                                                             H                                         Methyl    Methyl    H        C.sub.2 H.sub.5 S                                                                      Methyl                                    Methyl    Methyl    H        Cyclopropyl                                       Methyl     Methyl   Methyl   H       H                                         ______________________________________                                    

    ______________________________________                                          ##STR111##                                                                    Formula IE where Z is Sidechain ZB                                             D.sup.1 -D.sup.2                                                                           R.sup.4  R.sup.5   Z.sup.5                                                                               Z.sup.8                                  ______________________________________                                         (CH.sub.2).sub.2                                                                           H        H         H      H                                        (CH.sub.2).sub.4                                                                           H        H         H      H                                        (CH.sub.2).sub.5                                                                           H        H         H      H                                        ______________________________________                                    

    ______________________________________                                          ##STR112##                                                                    Formula IE where Z is Sidechain ZB                                             D.sup.1 -D.sup.2                                                                           R.sup.4  R.sup.5  Z.sup.5 Z.sup.8                                  ______________________________________                                         CH.sub.2OCH.sub.2                                                                          H        H        H       H                                        (CH.sub.2).sub.2OCH.sub.2                                                                  H        H        H       H                                        CH.sub.2SCH.sub.2                                                                          H        Methyl   H       Methyl                                   CH.sub.2NHCH.sub.2                                                                         H        Methyl   H       H                                        (CH.sub.2).sub.2OCH.sub.2                                                                  Methyl   Methyl   H       Methyl                                   (CH.sub.2).sub.3OCH.sub.2                                                                  Methyl   Methyl   H       H                                        (CH.sub.2).sub.2                                                                           H        Methyl   Methyl  H                                        (CH.sub.2).sub.3                                                                           H        Methyl   Methyl  H                                        (CH.sub.2).sub.3                                                                           H        Methyl   Ethyl   H                                        (CH.sub.2).sub.3                                                                           H        H        n-Propyl                                                                               H                                        (CH.sub. 2).sub.4                                                                          H        H        Methyl  H                                        (CH.sub.2).sub.4                                                                           H        H        Ethyl   Methyl                                   (CH.sub.2).sub.3                                                                           H        H        n-Hexyl Methyl                                   ______________________________________                                    

    ______________________________________                                          ##STR113##                                                                    Formula IE where Z is Sidechain ZE                                             R.sup.1    Z.sup.5  Z.sup.6     Z.sup.7                                        ______________________________________                                         Methyl     H        H           H                                              Methyl     H        3-Methyl    H                                              Methyl     H        6-Methyl    H                                              Methyl     H        5-t-Butyl   H                                              Methyl     H        5-Methyl    6-Methyl                                       Methyl     H        5-Methoxy   H                                              Methyl     H        4-COOH      H                                              ______________________________________                                    

    ______________________________________                                          ##STR114##                                                                    Formula IE where Z is Sidechain ZE                                             R.sup.1    Z.sup.5    Z.sup.6     Z.sup.7                                      ______________________________________                                         Methyl     H          4-Chloro    H                                            Methyl     H          5-Chloro    H                                            Ethyl      H          5-Bromo     6-Bromo                                      n-Propyl   H          5-Nitro     H                                            n-Butyl    H          6-Nitro     H                                            Methyl     Methyl     3-Methyl    H                                            Methyl     Methyl     6-Methyl    H                                            Methyl     Methyl     5-t-Butyl   H                                            Methyl     Methyl     5-Methyl    6-Methyl                                     Methyl     Methyl     5-Methoxy   H                                            Methyl     Methyl     4-COOH      H                                            Methyl     Methyl     4-Chloro    H                                            Methyl     Methyl     5-Chloro    H                                            Methyl     Methyl     5-Bromo     6-Bromo                                      Methyl     Methyl     6-Nitro     H                                            Methyl     n-Propyl   H           H                                            Methyl     n-Propyl   3-Methyl    H                                            Methyl     n-Propyl   6-Methyl    H                                            Methyl     n-Propyl   5-t-Butyl   H                                            Methyl     n-Propyl   5-Methyl    6-Methyl                                     Methyl     n-Propyl   5-Methoxy   H                                            Methyl     n-Propyl   4-COOH      H                                            Methyl     n-Propyl   4-Chloro    H                                            Methyl     n-Propyl   5-Chloro    H                                            Methyl     n-Propyl   5-Bromo     6-Bromo                                      Methyl     n-Propyl   6-Nitro     H                                            ______________________________________                                    

    ______________________________________                                          ##STR115##                                                                    Formula IE where Z is Sidechain ZH                                             R.sup.1        D.sup.4      Z.sup.1                                            ______________________________________                                         Methyl         CH.sub.2     Methyl                                             Methyl         OCH.sub.2    Methyl                                             Methyl         CH.sub.2     Ethyl                                              Methyl         CH.sub.2     n-Propyl                                           Ethyl          (CH.sub.2).sub.2                                                                            H                                                  n-Propyl       (CH.sub.2).sub.2                                                                            Methyl                                             N-Butyl        (CH.sub.2).sub.2                                                                            Ethyl                                              Methyl         (CH.sub.2).sub.3                                                                            H                                                  Methyl         (CH.sub.2).sub.3                                                                            Methyl                                             Methyl         CH.sub.2     CF.sub.3                                           ______________________________________                                    

Example 23 (E)-2-(2-{2-[1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-]ethylidenecyclopent-1-(S)-yl)}acetic acid

10A. Methyl (E)-6-(1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate

A solution of (E)-6-(1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid in methanol (200 ml) was treated with p-toluenesulfonic acid (0.8 g) and stirred at 25° C. for 16 hours. The reaction mixture was cooled to 0° C. Methyl (E)-6-(1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate, m.p. 116.5-117.6, was collected by filtration.

10B. Methyl (E)-6-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate

A solution of methyl (E)-6-(1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate (8.61 g) and imidazole (3.5 g) in dimethyl formamide (40 ml) was treated with t-butyldimethylsilyl chloride (4.50 g) and stirred at 25° C. for 14 hours. The reaction mixture was then poured into ice water and extracted with ether. Drying over magnesium sulfate and evaporation gave methyl (E)-6-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate.

10C. 2-(4-t-Butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-acetaldehyde

A solution of methyl (E)-6-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate (10.6 g) in methylene chloride (150 ml), methanol (150 ml), and pyridine (5 ml) was treated with an excess of ozone at -70° C. The reaction was quenched with dimethylsulfide (20 ml) and stirred for 5 hours at 25° C. The reaction mixture was poured into 1N aqueous sodium hydrogen sulfate. Extraction with 1:1 ethyl acetate:hexane gave an oil which on purification by silica gel chromatography gave 2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-acetaldehyde, m.p. 90.9°-91.6° C.

10D. dl-1-[2-(4-t-Butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-1-hydroxy-1-yl]cyclopent-1-ene

A solution of 1-bromocyclopentene (21.4 g) in tetrahydrofuran (100 ml) was added over 30 minutes to magnesium (3.62 g) in tetrahydrofuran (30 ml). The reaction mixture was refluxed for 15 minutes and then diluted with tetrahydrofuran so that the final volume was 200 ml. This Grignard reagent (31 ml) was then added to a solution of 2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-acetaldehyde in tetrahydrofuran (100 ml) at -65° C. After 40 minutes the reaction mixture was poured into aqueous ammonium chloride. Extraction with ether gave an oil which was recrystalized from t-butylmethyl ether/hexane to give dl-1-[2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-1-hydroxy-1-yl]cyclopent-1-ene, m.p. 129.5°-132° C.

10E. Cyclopentyl (4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisbenzofuran-5-yl methyl)methanone

A solution of dimethyl sulfoxide (3 ml) in methylene chloride (100 ml) was cooled to -60° C. and treated with trifluoroacetic anhydride (4 ml). dl-1-[2-(4-t-Butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-1-hydroxy-1-yl]cyclopent-1-ene (4.1 g) in methylene chloride (14 ml) was added over 5 minutes and the reaction mixture was stirred at -60° C. for 1 hour. Triethylamine (11 ml) was added and the reaction mixture was allowed to warm to 20° C. Aqueous workup and extraction with methylene chloride, evaporation of the solvent, and crystallization of the residue from t-butylmethyl ether gave cyclopentyl (4-t-butyl-dimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl methyl) methanone, m.p. 128.2°-129.4° C.

10F. (S)-2-(4-t-Butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-1-cyclopentenyl-1-hydroxyethane

Cyclopentyl (4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl methyl)methanone (4.2 g) was treated with a 1M toluene solution of (R)-tetrahydro-1-methyl-3,3-diphenyl-1H,3H-pyrrolo-[1,2-c][1,3,2]oxazaborole (3 ml). The toluene was evaporated in vacuo and methylene chloride added (2 ml). The reaction mixture was cooled to -30° C. and borane/dimethyl sulfide (0.33 ml) was added three times at 45 minute intervals. The reaction mixture was stirred 16 hours at -30° C. and quenched by addition of 1M hydrogen chloride/ether (3 ml). Toluene was added (10 ml) and the solution filtered, diluted with ether (200 ml), washed with aqueous hydrochloric acid, aqueous sodium bicarbonate and brine. Drying and evaporation gave an oil which was purified by silica gel chromatography to give (S)-2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-1-cyclopentenyl-1-hydroxyethane. Further purification by crystallization from t-butylmethyl ether gave material with an enantiomeric excess of 97.8% (Chiracel OD-H, 85:15 hexane:i-propanol, 0.8 ml/minute, minor 8.3 minutes, major 9.2 minutes).

10G. Ethyl (S)(E)-2-{2-[2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopent-1-yl}acetate

A mixture of (S)-2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-1-cyclopentenyl-1-hydroxyethane (2.8 g), pivalic acid (0.1 g) and triethyl orthoacetate (125 ml) was heated to 138° C. After 2.5 hours, more pivalic acid (65 mg) was added and the reaction was continued 1 hour more. The reaction mixture was cooled, the excess triethyl orthoacetate removed in vacuo, and the residue chromatographed on silica gel (20% ethyl acetate/hexane) to give ethyl (S)(E)-2-{2-[2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopent-1-yl}acetate.

10H. Ethyl (S)(E)-2-{2-[2-(1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)ethylidenelcyclopent-1-yl}acetate

A solution of ethyl (S)(E)-2-{2-[2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopent-1-yl}acetate (1.24 g) in tetrahydrofuran (8 ml) was cooled to 0° C. and treated with 1M tetrabutylammonium fluoride in tetrahydrofuran (3 ml). After 5 minutes, the reaction mixture was poured into ice water and extracted with ethyl acetate. The extracts were dried, evaporated and the residue chromatographed on silica gel (20% ethyl acetate/hexane) to give ethyl (S)(E)-2-{2-[2-(1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopent-1-yl}acetate, m.p. 95.0°-95.7° C.

10I. (S)(E)-2-{2-[2-(1,3-Dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl]ethylidene]cyclopent-1-yl}acetic acid

A mixture of ethyl (S)(E)-2-{2-[2-(1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopent-1-yl}acetate (0.4 g) in methanol (20 ml) and water (20 ml) was treated with lithium hydroxide (1.6 g). The reaction mixture was heated at 65° C. for 2 hours and then cooled. The methanol was removed in vacuo end the residue treated with excess 1M sodium hydrogen sulfate. Extraction with ethyl acetate followed by drying and evaporation gave a residue which was recrystalized from t-butylmethyl ether to give (S)(E)-2-{2-[2-(1,3-dihydro-6-ethyl-4-hydroxy-7-methyl-3-oxoisobenzofuran-5-yl)ethylidene]cyclopent-1-yl}acetic acid, m.p. 168.2°-169.3° C. with an enantiomeric excess of 96.4% (Chiracel AD, 85:15 hexane:i-propanol, 0.1% trifluoroacetic acid, 0.8 ml/minute, minor 12.6 minutes, major 13.5 minutes).

Example 24

This example illustrates the preparation of a representative pharmaceutical formulation for oral administration containing an active compound of Formula I, e.g., (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

    ______________________________________                                                          Quantity per                                                  Ingredients      tablet, mgs.                                                  ______________________________________                                         Active Compound  200                                                           Lactose, spray-dried                                                                            148                                                           Magnesium stearate                                                                              2                                                             ______________________________________                                    

The above ingredients are mixed and introduced into a hard-shell gelatin capsule.

Other compounds of Formula I, such as those prepared in accordance with Examples 15-23, can be used as the active compound in the preparation of the orally administrable formulations of this example.

Example 25

This example illustrates the preparation of another representative pharmaceutical formulation for oral administration containing an active compound of Formula I, e.g., (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

    ______________________________________                                                           Quantity per                                                 Ingredients       tablet, mgs.                                                 ______________________________________                                         Active Compound   400                                                          Cornstarch        50                                                           Croscarmellose sodium                                                                            25                                                           Lactose           120                                                          Magnesium stearate                                                                               5                                                            ______________________________________                                    

The above ingredients are mixed intimately and pressed into single scored tablets.

Other compounds of Formula I, such as those prepared in accordance with Examples 15-23, can be used as the active compound in the preparation of the orally administrable formulations of this example.

Example 26

This example illustrates the preparation of a representative pharmaceutical formulation containing an active compound of Formula I, e.g., (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

An oral suspension is prepared having the following composition.

    ______________________________________                                         Ingredients                                                                    ______________________________________                                         Active Compound       1.0       g                                              Fumaric acid          0.5       g                                              Sodium chloride       2.0       g                                              Methyl paraben        0.15      g                                              Propyl paraben        0.05      g                                              Granulated sugar      25.5      g                                              Sorbitol (70% solution)                                                                              12.85     g                                              Veegum K (Vanderbilt Co.)                                                                            1.0       g                                              Flavoring             0.035     ml                                             Colorings             0.5       mg                                             Distilled water       q.s. to 100                                                                              ml                                             ______________________________________                                    

Other compounds of Formula I, such as those prepared in accordance with Examples 15-23, can be used as the active compound in the preparation of the orally administrable formulations of this example.

Example 27

This example illustrates the preparation of a representative pharmaceutical formulation for oral administration containing an active compound of Formula I, e.g., (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

An injectable preparation buffered to a suitable pH is prepared having the following composition:

    ______________________________________                                         Ingredients                                                                    ______________________________________                                         Active Compound         0.2       g                                            Sodium Acetate Buffer Solution (0.4M)                                                                  2.0       ml                                           HCL (1N) or NaOH (1N)   q.s. to pH 4                                           Water (distilled, sterile)                                                                             q.s. to 20 ml                                          ______________________________________                                    

Other compounds of Formula I, such as those prepared in accordance with Examples 15-23, can be used as the active compound in the preparation of the injectable formulations of this example.

Example 28

This example illustrates the preparation of a representative pharmaceutical formulation for topical application containing an active compound of Formula I, e.g., (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

    ______________________________________                                         Ingredients          grams                                                     ______________________________________                                         Active compound      0.2-10                                                    Span 60              2                                                         Tween 60             2                                                         Mineral oil          5                                                         Petrolatum           10                                                        Methyl paraben       0.15                                                      Propyl paraben       0.05                                                      BHA (butylated hydroxy anisole)                                                                     0.01                                                      Water                q.s. to 100                                               ______________________________________                                    

All of the above ingredients, except water, are combined and heated to 60° C. with stirring. A sufficient quantity of water at 60° C. is then added with vigorous stirring to emulsify the ingredients, and water then added q.s. 100 g.

Other compounds of Formula I, such as those prepared in accordance with Examples 15-23, can be used as the active compound in the preparation of the topical formulations of this example.

Example 29

This example illustrates the preparation of a representative pharmaceutical formulation containing an active compound of Formula I, e.g., (E)-6-(4-amino-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid.

A suppository totalling 2.5 grams is prepared having the following composition:

    ______________________________________                                         Ingredients                                                                    ______________________________________                                         Active Compound  500 mg                                                        Witepsol H-15*   balance                                                       ______________________________________                                          (*triglycerides of saturated vegetable fatty acid; a product of                RichesNelson, Inc., New York, N.Y.)                                      

Other compounds of Formula I, such as those prepared in accordance with Examples 15-23, can be used as the active compound in the preparation of the suppository formulations of this example.

Example 30 In vitro Determination of Therapeutic Activity (As an Anti-Inflammatory, Anti-Viral, Anti-Tumor, Anti-Psoriatic and/or Immunosuppressive Agent) Utilizing the Inhibition of IMP Dehydrogenase Assay

This assay is a modification of the method of Anderson, J. H. and Sartorelli, A. C., Jour. Biol. Chem, 243z4762-4768 (1968). It measures the formation of NADH (λ_(max) =340 nm, ε340=6,220 M¹ cm¹) as Inosine 5'-monophosphate ("IMP") is converted to Xanthosine 5'-monophosphate ("XMP") by the human Type II IMP dehydrogenase ("IMPDH").

Compounds are dissolved and diluted in DMSO, and reaction solutions containing compounds at 0, 0.01, 0.10, 1.0, 10, and 100 μM are prepared in disposable methacrylic plastic microcuvets (`UV-transparent` plastic, 1 cm pathlength, 1.5 ml capacity). The solutions (0.5-1 ml) contain the following 0.1M TrisHCL, pH 8.0; 0.1M KCL; 3.0 mM EDTA; 100 μg/ml BSA; 0.05 mM IMP; 0.10 mM NAD; 10% DMSO; 5-15 nM IMPDH (0,003-0,010 units/ml; one unit of enzyme catalyzes the formation of one μmol NADH per minute at 40° C. at saturating substrate concentrations -200 μM IMP and 400 μM NAD). Reactions are performed at 40° C. and initiated by the addition of enzyme. Mycophenolic acid (IC₅₀ ≈0.02 μM) serves as the positive control. The reactions are monitored at 340 nm for 10 minutes in a UV/VIS spectrophotometer, and rate data are collected.

The 50% inhibitory value ("IC₅₀ ") is determined by fitting the fractional activities relative to control to the following equation on a Macintosh computer by the program Systat:

    Fractional activity=MAX/((X/IC.sub.50).sup.a +1).

X is the concentration of the compound, and the term n accounts for deviations of the data from a simple competitive inhibition model.

The compounds of the present invention inhibit IMPDH when tested by this method, indicating their activity as anti-inflammatory, anti-viral, anti-tumor, anti-psoriatic and/or immunosuppressive agents.

Example 31 In Vitro Determination of Immunosuppressive Activity Utilizing Responses of Human Peripheral Blood Lymphocytes to T- and B-cell Mitogens

This procedure is a modification of a procedure initially described by Greaves, et al. ["Activation of human T and B lymphocytes by polyclonal mitogens," Nature, 248:698-701 (1974)].

Human mononuclear cells ("PBL") are separated from heparinized whole blood by density gradient centrifugation in Ficoll-Plague (Pharmacia). After washing, 2×10⁵ cells/well are cultured in microtiter plates with RPMI 1640 supplemented with 5% fetal calf serum, penicillin and streptomycin. PHA (Sigma) at 10 μg/ml is then added. Test materials are tested at concentrations between 10⁴ and 10⁸, by addition to the culture at time 0. Cultures are set up in guadruplicate and incubated at 37° C. in a humidified atmosphere with 7% CO₂ for 72 hours. A pulse of 0.5 μCi/well of ³ H-thymidine is added for the last 6 hours. Cells are collected on glass fiber filters with an automatic harvester and radioactivity is measured by standard scintillation procedures. The 50% inhibitory concentration ("IC₅₀ ") for mitogenic stimulation is determined graphically.

The compounds of the present invention show immunosuppressive activity when tested by this method.

Example 32 Determination of Immunosuppressive Activity Utilizing the Hemolytic Plaque Forming Cell Assay

This procedure is a modification of "The agar plaque technique for recognizing antibody producing cells," a procedure initially described by Jerne et al., [Cellbound Antibodies, Amos and Kaprowski editors (Wistar Institute Press, Philadelphia, 1963), p. 109].

Groups of 5-6 adult C578B1/6 male mice were sensitized with 1×10^(s) sheep red blood cells ("SRBC") and simultaneously treated with an oral dosage form of the test material in an aqueous vehicle. Animals in a control group receive the same volume of vehicle. Four days after SRBC inoculation, spleens are dispersed in loose Ten Broeck homogenizers. The number of nucleated cells ("WBC") is determined and the spleen cell suspension is mixed with SRBC, guinea pig complement and agar solution at 0.5% concentration. Aliquots of the above mixture (0.1 ml) are dropped on four separate quadrants of a Petri dish and are covered with cover slips. After two hours incubation at 37° C., areas of hemolysis around plaque-forming cells ("PFC") are counted with a dissecting microscope. Total WBC/spleen, PFC/spleen and PFC/10⁶ WBC ("PPM") are calculated for each mouse spleen. Geometric means of each treatment group are then compared with the vehicle-treated control group.

The compounds of the present invention show immunosuppressive activity when tested by this method.

While the present invention has been described with reference to the specific embodiments thereof, it should be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the true spirit and scope of the invention. In addition, many modifications may be made to adapt a particular situation, material, composition of matter, process, process step or steps, to the objective, spirit and scope of the present invention. All such modifications are intended to be within the scope of the claims appended hereto. 

What is claimed is:
 1. A method for treating a mammal having a disease state that is alleviated by treatment with an IMPDH inhibitor, which comprises administering to a mammal in need thereof a therapeutically effective amount of a compound represented by the formula: ##STR116## wherein: R¹ is hydrogen or lower alkyl;R² is hydrogen, lower alkyl, --C(O)R³, --C(O)NR⁴ R⁵, --CO₂ R⁶, or --SO₂ R³ ; in which:R³ is hydrogen, lower alkyl, halo lower alkyl or optionally substituted phenyl; R⁴ is hydrogen, lower alkyl or optionally substituted phenyl; R⁵ is hydrogen, lower alkyl or optionally substituted phenyl; R⁶ is lower alkyl or optionally substituted phenyl; and R⁷ is lower alkyl, cycloalkyl, fluorovinyl, difluorovinyl, trifluorovinyl, lower alkenyl, --C.tbd.C--R⁸, allyl, CHO, or CH₂ OR⁹ ; in which:R⁸ is hydrogen or lower alkyl, and R⁹ is hydrogen or 4-methoxybenzyl; and Z is a side chain selected from Formulae ZA, ZB, ZC, ZD, ZE, ZF, ZG, and ZH: ##STR117## wherein: Z¹ is hydrogen, lower alkyl, halo or CF₃ ; Z² is hydrogen, lower alkyl, lower alkoxy, aryl, or --CH₂ Z¹³,where Z¹³ is aryl or heteroaryl; Z³ is hydrogen, lower alkyl, lower alkenyl, lower alkoxy, phenyl, or --S(O)_(m) Z¹², where Z¹² is lower alkyl, and m is 0, 1 or 2; Z⁴ is hydrogen, lower alkyl, or phenyl,or Z³ and Z⁴ taken together with the carbon to which they are attached form cycloalkyl of three to five carbon atoms; and G is OH, lower alkoxy, lower thioalkyl, --NG¹ G², --O(CH₂)_(n) NG¹ G², --O(CH₂)_(n) NG¹ G², or --O(CH₂)_(n) N═G³, wheren is an integer from 1 to 6, G¹ is hydrogen or lower alkyl, G² is hydrogen or lower alkyl, and =G³ is lower alkylene of four to six carbon atoms, or lower alkylene of three to five carbon atoms plus one member that is --O--, --S--, or --N(G⁴)-- where G⁴ is hydrogen or lower alkyl; ##STR118## wherein: Z⁵ is hydrogen or lower alkyl; Z⁸ is hydrogen or lower alkyl; D¹ and D² together with their adjacent carbon atoms form an optionally substituted, saturated or unsaturated carbocyclic or heterocyclic ring of 3 to 7 atoms; and G is as defined above; or ##STR119## wherein: Z⁵, Z⁸, and G are as defined above; or ##STR120## wherein: D³ is --CH₂ -- or --CH₂ CH₂ --; and G is as defined above; or ##STR121## wherein: Z⁶ is hydrogen, lower alkyl, lower alkoxy, --COOH, --NH₂ or halo; Z⁷ is hydrogen, lower alkyl, lower alkoxy or halo; and Z⁵ and G are as defined above; or ##STR122## wherein: Z¹ and G are as defined above; or ##STR123## wherein: D³, Z², Z³, Z⁴ and G are as defined above; or ##STR124## wherein: D⁴ is --CH₂ --, --CH₂ CH₂ --, --CH₂ CH₂ CH₂ --, --O--, or --OCH₂ --; and Z¹ and G are as defined above;or a pharmaceutically acceptable salt thereof.
 2. The method of claim 1, wherein said disease state is allograft rejection.
 3. The method of claim 2 which comprises the relieving or inhibiting of allograft rejection.
 4. The method of claim 1, wherein said disease state is an inflammatory disorder. 